<p><strong>Clinical Research Coordinator (Contract Position)</strong></p><p><br></p><p><strong>Duration</strong>: Until December 2026</p><p><strong>Job Type: </strong>40 hours per week (Monday-Friday) - during normal business hours</p><p><strong>Start Date: </strong>ASAP</p><p><br></p><p><strong>Job Description:</strong></p><p><strong>We are seeking a full-time, onsite Clinical Research Coordinator (CRC) </strong>with experience in clinical research to support an ongoing <strong>Oncology </strong>clinical trial. The ideal candidate will be able to work independently and act as one of the main CRCs for this study.</p><p><br></p><p><strong>Key Responsibilities:</strong></p><p>Patient Recruitment: Identify and recruit suitable patients for the clinical trial.</p><p>Medical Record Review: Conduct thorough reviews of patient medical records.</p><p>Participant Screening: Perform phone screenings or prescreen participants for eligibility.</p><p>Informed Consent: Obtain informed consent from trial participants.</p><p>Data Management: Collect study data and enter it into electronic data capture (EDC) systems.</p><p>Query Resolution: Address and resolve data queries promptly.</p><p>Medical Record Retrieval: Obtain necessary medical records for the study.</p><p>Documentation: Create and maintain source documents.</p><p>Compliance: Ensure compliance with e-diary protocols.</p><p>Regulatory Support: Assist with Institutional Review Board (IRB) approvals and provide regulatory support.</p><p>Adverse Event Reporting: Assist with timely reporting of adverse events (AEs) and serious adverse events (SAEs).</p><p>Study Binder Maintenance: Keep study binders organized and up-to-date.</p><p>Participant Follow-Up: Conduct follow-up with study subjects to ensure retention.</p><p>Scheduling: Arrange in-patient visits and follow-up appointments, and send reminders.</p><p>Administrative Tasks: Perform various administrative duties as required.</p><p>Community Outreach: Networking with referral physicians, visiting clinics and hospitals to educate medical professionals and patients about the clinical trial, distributing study materials, posting recruitment materials, and maintaining online portals to track metrics.</p><p>Specimen Collection and Processing: Obtain biological specimens from participants, label and temporarily store them, perform initial processing like serum separation, and transport them to a lab for further analysis and storage.</p><p>General Support: Assist with any other study-related efforts as deemed necessary by the site.</p><p><br></p><p><strong>Qualifications:</strong></p><ul><li>Minimum of two years of experience as a Clinical Research Coordinator</li><li>Oncology experience required</li><li>Proficiency with electronic medical records (EMR) and electronic data capture (EDC) system</li></ul>

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Clinical Research Coordinator

<h1 style="text-align: center;"><strong>Job Title: Clinical Research Coordinator</strong></h1><p><br></p><p><strong>Position: CRC</strong></p><p><strong>Pay: $23-$28/hr</strong></p><p><br></p><p><strong>Top Skills Details:</strong></p><p><br></p><ul><li>2 Years of CRC experience MINIMUM</li><li>Experience in phases 1-3</li><li>Phlebotomy and sample processing preferred</li><li>Experience performing Cardiograms</li><li>Oncology, Urology and ENT experience is preferred</li></ul><p><br></p><p><strong>Job Description:</strong></p><p><br></p><ul><li>Under general supervision of the Research Director, coordinates and manages all aspects of clinical studies involved in prostate and bladder oncology, including but not limited to subject screening, recruitment, data entering, abstracting, and assessment.</li><li>Execute, manage, and coordinate research protocols, as directed by the Director of Research and/or Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols and regulating agency policies.</li><li>Support the management and coordinating the tasks of single or multiple clinical research studies, depending on their size and complexity; acting as an intermediary between services and departments while overseeing data and specimen collection; manage and report on study results, create, clean, update, and manage databases and comprehensive datasets as well as renewals and modifications of protocol applications and the implementation of new studies</li><li>Document and maintain required records necessary for study activities per local, state, and FDA GCP requirements</li></ul><p><br></p><p><strong>Work Environment:</strong></p><p><br></p><p>Schedule: Monday - Friday 8-5 no weekend, but they might need to come in a little earlier if needed but this is not common. Depends if</p><p>patients are coming in early. </p><p><br></p><p>Workload: CRC will be responsible for 5-7 trials at any given time. They are expecting to see 3-4 patients per day.</p><p><br></p><p>Please email : mscherlacher@ actalentservices.com with your updated resume!</p>

<h1><strong>Job Title: Research Coordinator</strong></h1><p><br></p><h2>Job Description</h2><p>The Research Coordinator will support an Investigator, Research Associate, or Project Manager in operationalizing tasks associated with implementing a research study. This involves various tasks related to recruitment, data collection, data management, and reporting of results.</p><p><br></p><h2>Responsibilities</h2><ul><li>Recruit and consent research participants.</li><li>Conduct telephone or in-person interviews with participants, including screening for eligibility.</li><li>Perform follow-up by telephone, email, and/or mail with study participants.</li><li>Prepare, mail, and process questionnaires and other study correspondence.</li><li>Assist in tracking study participants using MS Excel.</li><li>Maintain accurate and detailed records and files of work.</li><li>Review, edit, clean, and enter participant data into a database.</li><li>Assist with literature reviews for proposal submissions and manuscript preparation.</li><li>Perform bookkeeping related to study budgets, including ordering supplies, requesting checks for payment, and participant incentives.</li><li>Perform miscellaneous administrative tasks such as typing labels, copying, faxing, meeting preparation, note-taking, and transcribing audio files.</li></ul><h2>Essential Skills</h2><ul><li>High school diploma or General Education Development (GED)</li><li>6+ months of clinical research experience</li><li>Experience in the medical field, including phlebotomy and vaccines</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Tech savvy</li><li>Interest in growing in Clinical Research</li><li>Proficiency in data entry</li></ul>

<p style="text-align: center;"><strong>Clinical Research Coordinator</strong></p><p><strong>MUST be local to Ames, IA as interviews will be onsite!</strong></p><p><strong>MUST have patient facing Clinical Research Coordinator experience</strong></p><p><br></p><p><strong><u>Contract</u></strong></p><p>6 months with the potential for extension</p><p><br></p><p><strong><u>Clinical Research Coordinator</u></strong></p><p>Recruits and consents research participants.</p><p>Conducts telephone or in-person interviews with</p><p>participants, including screening for eligibility.</p><p>Performs follow-up by telephone, e-mail, and/or mail with</p><p>study participants.</p><p>Prepares, mails, and processes questionnaires and other</p><p>study correspondence.</p><p>Assists in tracking study participants using MS Excel.</p><p>Keeps accurate and detailed records and files of work.</p><p>Reviews, edits, cleans, and enters participant data into a</p><p>database.</p><p>May assist with literature reviews for proposal submissions</p><p>and manuscript preparation.</p><p>Handles bookkeeping related to study budgets, including</p><p>ordering supplies, requesting checks for payment, and participant incentives.</p><p>Performs miscellaneous administrative tasks such as typing</p><p>labels, copying, faxing, meeting preparation, note-taking, and transcribing</p><p>audio files.</p><p><br></p><p><strong><u>Qualifications</u></strong></p><p>1+ year of Clinical Research Coordinator (CRC) experience</p><p>Experience with chart review and patient recruitment</p><p>Knowledge of EDC and EMR systems</p><p>Understanding of clinical research and Good Clinical</p><p>Practice (GCP)</p><p>Experience in pre-screening patients</p><p>High school diploma or General Education Development (GED)</p><p>required</p><p>Vaccine experience is a plus</p><p>Phlebotomy experience is a plus</p><h1><br></h1><h1><br></h1>

<p style="text-align: center;"><b>Clinical Research Coordinator </b></p><p><br></p><p>The CRC collaborates with the Research Institute Division Manager, Principal Investigators, and key stakeholders to plan, coordinate, implement, and complete clinical trials and research projects. </p><p><strong>Key Responsibilities: </strong></p><p>Oversee and manage research studies focused on complex medical conditions.</p><p>Provide direct patient care under research protocols in collaboration with the PI and healthcare team.</p><p>Ensure compliance with study protocols, regulatory requirements, and ethical standards.</p><p>Coordinate study activities from initiation through close-out, including patient recruitment, informed consent, data collection, and reporting.</p><p>Process laboratory specimens per study requirements.</p><p><br></p><p><strong><u>Qualifications</u></strong></p><p>Must have a minimum of 3 years of  patient facing Clinical Research Coordinator experience </p><p>Bachelor&#39;s degree</p><p><br></p>

<h1><strong>Job Title: Clinical Research Coordinator - Charleston, SC</strong></h1><p><br></p><h2><strong>Job Description</strong></h2><p>The Research Coordinator will play a vital role in assisting an Investigator, Research Associate, or Project Manager with the operational tasks necessary for implementing a research study. This position involves various responsibilities related to participant recruitment, data collection, data management, and reporting of study results.</p><p><br></p><h2><strong>Responsibilities</strong></h2><ul><li>Recruit and obtain consent from research participants.</li><li>Conduct telephone or in-person interviews, including eligibility screening.</li><li>Perform follow-up with study participants via telephone, e-mail, or mail.</li><li>Prepare, mail, and process questionnaires and other study correspondence.</li><li>Assist in tracking study participants using MS Excel.</li><li>Maintain accurate and detailed records and files of work.</li><li>Review, edit, clean, and enter participant data into a database.</li><li>Assist with literature reviews for proposal submissions and manuscript preparation.</li><li>Handle bookkeeping related to study budgets, including ordering supplies and requesting checks for payment and participant incentives.</li><li>Perform miscellaneous administrative tasks such as typing labels, copying, faxing, meeting preparation, note-taking, and transcribing audio files.</li></ul><h2><strong>Required Skills &amp; Qualifications</strong></h2><ul><li>High school diploma or General Education Development (GED)</li><li>6+ months of clinical research experience</li><li>Backgroundin the medical field, including phlebotomy and vaccines</li><li>Tech-savvy</li><li>Interest in growing in clinical research</li><li>Data entry skills</li></ul><h1><br></h1>

<h1><strong>Job Title: Clinical Research Coordinator - Salisbury, NC</strong></h1><p><br></p><h2>Job Description</h2><p>The Research Coordinator plays a vital role in supporting research studies by assisting in the implementation and management of various tasks. This position involves a range of responsibilities, including participant recruitment, data collection and management, as well as reporting of study results.</p><p><br></p><h2>Responsibilities</h2><ul><li>Recruit and consent research participants.</li><li>Conduct telephone or in-person interviews with participants, including screening for eligibility.</li><li>Perform follow-up with study participants via telephone, email, or mail.</li><li>Prepare, mail, and process questionnaires and other study correspondence.</li><li>Assist in tracking study participants using MS Excel.</li><li>Maintain accurate and detailed records and files of work.</li><li>Review, edit, clean, and enter participant data into a database.</li><li>Assist with literature reviews for proposal submissions and manuscript preparation.</li><li>Handle bookkeeping related to study budgets, including ordering supplies and requesting payments for participant incentives.</li><li>Perform miscellaneous administrative tasks such as typing labels, copying, faxing, meeting preparation, note-taking, and transcribing audio files.</li></ul><h2>Essential Skills</h2><ul><li>High school diploma or GED.</li><li>6+ months of clinical research experience.</li><li>Experience in the medical field, including phlebotomy and vaccines.</li><li>Familiarity with chart review, patient recruitment, electronic data capture (EDC), electronic medical records (EMR), and Good Clinical Practice (GCP).</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Tech-savvy with an interest in growing in the field of clinical research.</li><li>Proficient in data entry.</li></ul>

<h1><strong>Job Title: Research Coordinator</strong></h1><p><br></p><h2>Job Description</h2><p>The Research Coordinator will assist in operationalizing tasks associated with implementing a research study. This role involves various tasks related to recruitment, data collection, data management, and the reporting of results.</p><p><br></p><h2>Responsibilities</h2><ul><li>Recruit and consent research participants.</li><li>Conduct telephone or in-person interviews with participants, including screening for eligibility.</li><li>Perform follow-up via telephone, email, and mail with study participants.</li><li>Prepare, mail, and process questionnaires and other study correspondence.</li><li>Assist in tracking study participants using MS Excel.</li><li>Maintain accurate and detailed records and files of work.</li><li>Review, edit, clean, and enter participant data into a database.</li><li>Assist with literature reviews for proposal submissions and manuscript preparation.</li><li>Handle bookkeeping related to study budgets, including ordering supplies and requesting checks for payment and participant incentives.</li><li>Perform miscellaneous administrative tasks such as typing labels, copying, faxing, meeting preparation, note-taking, and transcribing audio files.</li></ul><h2>Essential Skills</h2><ul><li>High school diploma or General Education Development (GED).</li><li>6+ months of clinical research experience.</li><li>Experience in the medical field, including phlebotomy and vaccines.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Tech savvy.</li><li>Interest in growing in Clinical Research.</li><li>Proficiency in data entry.</li></ul>

<h1><strong>Job Title: Clinical Research Coordinator</strong></h1><h2><strong>Job Description</strong></h2><p>The Research Coordinator will support the implementation of research studies by assisting with various tasks related to recruitment, data collection, data management, and reporting of results.</p><p><br></p><h2><strong>Responsibilities</strong></h2><ul><li>Recruit and consent research participants.</li><li>Conduct telephone or in-person interviews with participants, including screening for eligibility.</li><li>Perform follow-up with study participants through telephone, e-mail, or mail.</li><li>Prepare, mail, and process questionnaires and other study correspondence.</li><li>Assist in tracking study participants using MS Excel.</li><li>Maintain accurate and detailed records and files of work.</li><li>Review, edit, clean, and enter participant data into a database.</li><li>Assist with literature reviews for proposal submissions and manuscript preparation.</li><li>Handle bookkeeping related to study budgets, including ordering supplies and requesting checks for payment and participant incentives.</li><li>Perform miscellaneous administrative tasks such as typing labels, copying, faxing, meeting preparation, note-taking, and transcribing audio files.</li></ul><h2><strong>Essential Skills</strong></h2><ul><li>High school diploma or General Education Development (GED).</li><li>Minimum of 6 months of clinical research experience.</li><li>Experience in the medical field</li></ul><h2><strong>Additional Skills &amp; Qualifications</strong></h2><ul><li>Phlebotomy skills (Preferred).</li><li>Tech savvy.</li><li>Interest in growing in Clinical Research.</li><li>Experience in data entry.</li></ul>

<h1><strong>Title: Clinical Research Coordinator III</strong></h1><p><br></p><h2>Job Description</h2><p>The Clinical Research Coordinator III is an experienced clinical research professional responsible for leading the planning, implementation, monitoring, and evaluation of multiple clinical research protocols. This role involves managing daily operations of multiple studies, ensuring the integrity of each study, and mentoring less experienced Clinical Research Coordinators. The coordinator will maximize adherence to research standards and regulatory guidelines, work closely with study team members to ensure participant safety, manage administrative tasks, and facilitate information flow.</p><p><br></p><h2>Responsibilities</h2><ul><li>Coordinate the implementation of multiple complex clinical research protocols.</li><li>Develop standard operating procedures (SOPs) and templates with guidance from the Principal Investigator or Clinical Research Manager.</li><li>Oversee eligibility screening and recruitment activities, implementing strategies to increase participant accrual.</li><li>Manage sample processing, packing, and shipping according to protocol and applicable standards.</li><li>Plan and operationalize strategies to monitor, document, report, and follow up on unanticipated occurrences and protocol deviations.</li><li>Develop preventive and corrective actions for protocol deviations.</li><li>Ensure adherence to study-related clinical research best practices and scientific manuals.</li><li>Lead protocol implementation and study progress, keeping investigators informed.</li><li>Identify and resolve ethical conflicts arising during protocol implementation, referring issues to the Research Ethics Team as needed.</li><li>Organize and manage site visits and internal/external auditing activities.</li><li>Coordinate research team meetings and ensure effective communication across the board.</li><li>Synchronize study visits, procedures, and clinical tests with data collection schedules and manage participant progress.</li><li>Compile information for research reports and peer-reviewed publications and develop strategies to disseminate findings.</li><li>Adhere to fundamental requirements of international, national, and local regulatory bodies.</li><li>Maintain requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.</li><li>Safeguard assets according to unit-level policies and procedures.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree required.</li><li>Open to foreign MDs with the right credentials.</li><li>Minimum of 4-5 years of solid experience as a Clinical Research Coordinator managing and running trials within oncology.</li><li>Certification as a Clinical Research Coordinator III is required, with ACRP/SOCRA certification preferred or willingness to obtain within six months of employment.</li></ul><h2>Work Environment</h2><p>This position is primarily in-office from Monday to Friday, with the possibility of working two days from home if not seeing patients. Work hours are from 8 AM to 5 PM.</p><p><br></p><p style="text-align: center;"><br></p>

Clinical Research Coordinator III

<h1><strong>Job Title: Clinical Research Coordinator III</strong></h1><p><br></p><h2>Job Description</h2><p>The Clinical Research Coordinator III is an experienced clinical research professional responsible for leading the planning, implementation, monitoring, and evaluation of multiple clinical research protocols. This role involves managing daily operations of multiple studies, ensuring the integrity of each study, and mentoring less experienced Clinical Research Coordinators. The coordinator will maximize adherence to research standards and regulatory guidelines, work closely with study team members to ensure participant safety, manage administrative tasks, and facilitate information flow.</p><p><br></p><h2>Responsibilities</h2><ul><li>Coordinate the implementation of multiple complex clinical research protocols.</li><li>Develop standard operating procedures (SOPs) and templates with guidance from the Principal Investigator or Clinical Research Manager.</li><li>Oversee eligibility screening and recruitment activities, implementing strategies to increase participant accrual.</li><li>Manage sample processing, packing, and shipping according to protocol and applicable standards.</li><li>Plan and operationalize strategies to monitor, document, report, and follow up on unanticipated occurrences and protocol deviations.</li><li>Develop preventive and corrective actions for protocol deviations.</li><li>Ensure adherence to study-related clinical research best practices and scientific manuals.</li><li>Lead protocol implementation and study progress, keeping investigators informed.</li><li>Identify and resolve ethical conflicts arising during protocol implementation, referring issues to the Research Ethics Team as needed.</li><li>Organize and manage site visits and internal/external auditing activities.</li><li>Coordinate research team meetings and ensure effective communication across the board.</li><li>Synchronize study visits, procedures, and clinical tests with data collection schedules and manage participant progress.</li><li>Compile information for research reports and peer-reviewed publications and develop strategies to disseminate findings.</li><li>Adhere to fundamental requirements of international, national, and local regulatory bodies.</li><li>Maintain requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.</li><li>Safeguard assets according to unit-level policies and procedures.</li></ul><h2>Essential Skills</h2><ul><li>Research analysis in oncology.</li><li>Clinical research certification.</li><li>Experience with patient records and institutional review boards (IRB).</li><li>Experience in clinical trials, oncology, clinical research, and electronic data capture (EDC).</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree required.</li><li>Open to foreign MDs with the right credentials.</li><li>Minimum of 4-5 years of solid experience as a Clinical Research Coordinator managing and running trials within oncology.</li><li>Certification as a Clinical Research Coordinator III is required, with ACRP/SOCRA certification preferred or willingness to obtain within six months of employment.</li></ul><h2>Work Environment</h2><p>This position is primarily in-office from Monday to Friday, with the possibility of working two days from home if not seeing patients. Work hours are from 8 AM to 5 PM.</p><p><br></p><p>Recruiter Myles Laney</p>

<h1><strong>Job Title: Clinical Research Coordinator III</strong></h1><p><br></p><h2>Job Description</h2><p>The Clinical Research Coordinator III is an experienced clinical research professional responsible for leading the planning, implementation, monitoring, and evaluation of multiple clinical research protocols. This role involves managing daily operations of multiple studies, ensuring the integrity of each study, and mentoring less experienced Clinical Research Coordinators. The coordinator will maximize adherence to research standards and regulatory guidelines, work closely with study team members to ensure participant safety, manage administrative tasks, and facilitate information flow.</p><p><br></p><h2>Responsibilities</h2><ul><li>Coordinate the implementation of multiple complex clinical research protocols.</li><li>Develop standard operating procedures (SOPs) and templates with guidance from the Principal Investigator or Clinical Research Manager.</li><li>Oversee eligibility screening and recruitment activities, implementing strategies to increase participant accrual.</li><li>Manage sample processing, packing, and shipping according to protocol and applicable standards.</li><li>Plan and operationalize strategies to monitor, document, report, and follow up on unanticipated occurrences and protocol deviations.</li><li>Develop preventive and corrective actions for protocol deviations.</li><li>Ensure adherence to study-related clinical research best practices and scientific manuals.</li><li>Lead protocol implementation and study progress, keeping investigators informed.</li><li>Identify and resolve ethical conflicts arising during protocol implementation, referring issues to the Research Ethics Team as needed.</li><li>Organize and manage site visits and internal/external auditing activities.</li><li>Coordinate research team meetings and ensure effective communication across the board.</li><li>Synchronize study visits, procedures, and clinical tests with data collection schedules and manage participant progress.</li><li>Compile information for research reports and peer-reviewed publications and develop strategies to disseminate findings.</li><li>Adhere to fundamental requirements of international, national, and local regulatory bodies.</li><li>Maintain requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.</li><li>Safeguard assets according to unit-level policies and procedures.</li></ul><h2>Essential Skills</h2><ul><li>Research analysis in oncology.</li><li>Clinical research certification.</li><li>Experience with patient records and institutional review boards (IRB).</li><li>Experience in clinical trials, oncology, clinical research, and electronic data capture (EDC).</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree required.</li><li>Open to foreign MDs with the right credentials.</li><li>Minimum of 4-5 years of solid experience as a Clinical Research Coordinator managing and running trials within oncology.</li><li>Certification as a Clinical Research Coordinator III is required, with ACRP/SOCRA certification preferred or willingness to obtain within six months of employment.</li></ul><h2>Work Environment</h2><p>This position is primarily in-office from Monday to Friday, with the possibility of working two days from home if not seeing patients. Work hours are from 8 AM to 5 PM.</p><p><br></p><p style="text-align: center;"><strong><em>Send your resume to hjaquez@ actalentservices.com for more information. </em></strong></p>

<h1><strong>Job Title: Clinical Research Nurse</strong></h1><p><br></p><h2>Job Description</h2><p>Join a dynamic team focused on either Breast or Phase 1 solid tumor research at their main campus. Collaborate closely with a team of two other nurses and two coordinators, providing essential support in clinical settings.</p><p><br></p><h2>Responsibilities</h2><ul><li>Collaborate with coordinators to attend tumor boards and assist in patient identification.</li><li>Aid in the consenting process and development of treatment plans.</li><li>Work with pharmacy teams and providers for protocol approval.</li><li>Conduct follow-up blood draws and PK draws for outpatient pill treatments.</li><li>Coordinate with infusion nurses for follow-up draws in infusion cases.</li><li>Comfortably access and de-access patient ports.</li><li>Possibly perform EKGs, usually done by coordinators.</li><li>Provide training and guidance to the inpatient care team.</li><li>Coordinate with teams for data entry and regulatory tasks.</li></ul><h2>Essential Skills</h2><ul><li>Registered Nurse with a minimum of 2 years of experience.</li><li>Experience in Oncology or Clinical Research.</li><li>Proficiency in clinical care and clinical research.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Oncology Clinical Research certification or experience.</li></ul><h2>Work Environment</h2><p>The position is based in downtown Detroit. Employees enjoy a flexible start time between 7:00 and 9:00 AM, with schedules adaptable to patient needs. The role offers the opportunity to accrue four weeks of vacation in the first year.</p>

Clinical Research Nurse

<p style="text-align: center;"><strong>Clinical Research Nurse</strong></p><p><strong>Duties</strong></p><ul><li>Perform venipuncture, specimen processing, vital signs, electrocardiograms, IV infusions, and other protocol-required procedures.</li><li>Attend investigator meetings and site initiation visits to obtain training on drug preparation and administration.</li><li>Monitor for complications with study drug administration, focusing on injections or intravenous infusions.</li><li>Maintain accurate dispensing logs, including information such as lot number and drug vs. placebo.</li><li>Document laboratory data and adverse reactions, promptly notifying investigators and sponsors of unexpected events.</li><li>Assist other staff members based on research organization needs and priorities.</li><li>Actively recruit suitable patient participants for clinical trials, dedicating time each week for recruitment efforts.</li><li>Complete training on Clinical Trial Management System and maintain skills for database updates and participant reimbursement.</li><li>Communicate recruitment status and clinical needs to investigators and Site Manager.</li><li>Build relationships with monitors from sponsoring companies through various communication methods.</li><li>Proactively promote the site with monitors and in-house contacts for future trials.</li><li>Prepare study documentation for audits and assist auditors during audits.</li><li>Order clinical supplies and maintain protocol-specific rescue drugs, monitoring storage temperatures for safety.</li><li>Obtain and maintain knowledge of temperature monitoring devices and procedures for lab specimens and investigational products.</li><li>Maintain certification for packaging and shipping specimens on dry ice and update knowledge of lab procedures.</li><li>Act as OSHA Representative, maintaining employee immunization records and administering vaccines to staff.</li><li>Perform equipment calibration and maintain equipment calibration records.</li><li>Support training and additional development of clinical skills for site staff as needed.</li><li>Travel to other sites within the network as required to support workload increases or projects.</li></ul><p><strong>Essential Skills</strong></p><ul><li>MUST hold an active Illinois RN license</li><li>1+ year of prior CRC/CRN/Research experience OR 2+ years of nursing experience if no prior research</li><li>Experience in chart review, patient recruitment, and pre-screening patients</li><li>Proficiency in electronic data capture (EDC) and electronic medical records (EMR)</li><li>Knowledge of clinical research and Good Clinical Practice (GCP)</li><li>Phlebotomy and IV insertion experience</li></ul>

<h1><strong>Job Title: Clinical Research Nurse</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a dedicated Clinical Research Nurse to join our team. In this role, you will be responsible for recruiting, screening, and enrolling subjects into clinical trials. You will explain the informed consent process to participants and document any adverse events. Additionally, you will collect study documents, protocols, regulatory documents, informed consents, case report forms, and source documents. The preparation of Institutional Review Board (IRB) applications will also be part of your duties.</p><p><br></p><h2>Responsibilities</h2><ul><li>Recruit, screen, and enroll subjects into clinical trials.</li><li>Explain the informed consent process to participants.</li><li>Document adverse events during the trials.</li><li>Collect study documents, including protocols, regulatory documents, informed consents, case report forms, and source documents.</li><li>Prepare Institutional Review Board (IRB) applications.</li></ul><h2>Essential Skills</h2><ul><li>Experience with patient enrollment and consenting.</li><li>Knowledge of informed consent processes.</li><li>Experience in oncology clinical trials.</li><li>Proficiency with GCP, EDC, and clinical research coordination.</li><li>Chart review expertise.</li><li>2+ years of clinical research experience.</li><li>Experience with adverse event reporting.</li><li>Effective communication and writing skills.</li><li>Knowledge of IRB and human research protection regulations.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>BA/BS degree preferred.</li><li>Experience with in-hospital clinical research.</li><li>Oncology experience required </li></ul><h2>Work Environment</h2><p>This position offers a combination of an office and hospital/outpatient surgery setting. The work environment is fast-paced with a high volume workload involving industry and investigator studies. You will be part of one of the most prestigious academic research institutes in the world, equipped with state-of-the-art technology. The role involves working on high-profile studies with large, well-known sponsors.</p>

<h2><strong>Job Title: Clinical Research Nurse</strong></h2><p><br></p><h2>Job Description</h2><p>We are seeking a dedicated Clinical Research Nurse to perform technical and clinical requirements of study protocols. This includes venipuncture, specimen processing, vital signs, and more. This role also involves attending meetings to gain training on drug preparation and administration, monitoring for complications, maintaining accurate records, and assisting with audits.</p><p><br></p><h2>Responsibilities</h2><ul><li>Perform venipuncture, specimen processing, vital signs, electrocardiograms, IV infusions, IV pump operations, and other clinical procedures as needed for study protocols.</li><li>Attend investigator meetings, site initiation visits, and coordinator meetings to gain training on drug preparation and administration.</li><li>Obtain knowledge of study drugs, with emphasis on injection or intravenous infusion medications.</li><li>Monitor for complications with administration of study drugs, particularly injections or intravenous infusions.</li><li>Maintain accurate dispensing logs, including information such as lot number and drug vs. placebo.</li><li>Document laboratory data and adverse reactions, notifying investigators and relevant parties of any serious events.</li><li>Assist staff members as determined by organizational needs.</li><li>Actively recruit and sell services to patient participants for clinical trials.</li><li>Complete training on Clinical Trial Management System and maintain skills for database updates and participant reimbursement.</li><li>Communicate patient status, recruitment status, and study needs to investigators and Site Manager.</li><li>Build relationships with monitors from sponsoring companies and promote the site for future trials.</li><li>Prepare study documentation for audits and assist auditors.</li><li>Order and monitor clinical supplies and rescue drugs, ensuring proper documentation and maintenance.</li><li>Monitor and maintain temperatures of refrigerators, freezer units, and investigational product storage.</li><li>Act as OSHA Representative, maintaining employee immunization records and administering vaccines.</li><li>Perform equipment calibration and maintain calibration records.</li><li>Support training and development of clinical skills for site staff.</li><li>Travel to other sites within the network may be required to support workload increases and projects.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Must have an active RN license for the applicable state.</li><li>1+ years of prior CRC/CRN/Research experience is ideal.</li><li>If no prior research experience, a minimum of 2+ years of nursing experience is required.</li><li>IV Insertion experience is a huge plus.</li></ul><h2>Work Environment</h2><p>This position is on-site Monday to Friday, totaling 40 hours per week. You will be working with one of the leading healthcare providers in the US, offering opportunities for advancement within the organization.</p>

<p style="text-align: center;"><strong>Clinical Research Nurse-Contract</strong></p><p><strong>Duties</strong></p><ul><li>Perform venipuncture, specimen processing, vital signs, electrocardiograms, IV infusions, and other protocol-required procedures.</li><li>Attend investigator meetings and site initiation visits to obtain training on drug preparation and administration.</li><li>Monitor for complications with study drug administration, focusing on injections or intravenous infusions.</li><li>Maintain accurate dispensing logs, including information such as lot number and drug vs. placebo.</li><li>Document laboratory data and adverse reactions, promptly notifying investigators and sponsors of unexpected events.</li><li>Assist other staff members based on research organization needs and priorities.</li><li>Actively recruit suitable patient participants for clinical trials, dedicating time each week for recruitment efforts.</li><li>Complete training on Clinical Trial Management System and maintain skills for database updates and participant reimbursement.</li><li>Communicate recruitment status and clinical needs to investigators and Site Manager.</li><li>Build relationships with monitors from sponsoring companies through various communication methods.</li><li>Proactively promote the site with monitors and in-house contacts for future trials.</li><li>Prepare study documentation for audits and assist auditors during audits.</li><li>Order clinical supplies and maintain protocol-specific rescue drugs, monitoring storage temperatures for safety.</li><li>Obtain and maintain knowledge of temperature monitoring devices and procedures for lab specimens and investigational products.</li><li>Maintain certification for packaging and shipping specimens on dry ice and update knowledge of lab procedures.</li><li>Act as OSHA Representative, maintaining employee immunization records and administering vaccines to staff.</li><li>Perform equipment calibration and maintain equipment calibration records.</li><li>Support training and additional development of clinical skills for site staff as needed.</li><li>Travel to other sites within the network as required to support workload increases or projects.</li></ul><p><strong>Essential Skills</strong></p><ul><li>MUST hold an active Illinois RN license</li><li>1+ year of prior CRC/CRN/Research experience OR 2+ years of nursing experience if no prior research</li><li>Experience in chart review, patient recruitment, and pre-screening patients</li><li>Proficiency in electronic data capture (EDC) and electronic medical records (EMR)</li><li>Knowledge of clinical research and Good Clinical Practice (GCP)</li><li>Phlebotomy and IV insertion experience</li></ul>

<p><strong>Description</strong></p><p>We are seeking an RN to fill a support role on our clinical research team. This position will mentor multiple areas of our department and become proficient in various roles, including; research pharmacy, phlebotomy and research clinic. This position will fill various gaps in day-to-day operations. This role will require the candidate to:</p><p>- perform tasks such as; preparation of investigational products</p><p>- monitoring research subjects</p><p>-  taking and recording vital signs</p><p>- performing EKG’s, drawing blood for research and clinical lab samples</p><p>- recording study data in various data bases</p><p>- Verbal and written communication with the Principal Investigator, Sub-Investigators and Research Coordinators on site is a critical element of this role. Special projects to assist the department may be assigned as needed.</p><p><strong>Skills</strong></p><p>Clinical research, Clinical trial, Chart review</p><p><strong>Top Skills Details</strong></p><p>Clinical research,Clinical trial</p><p><strong>Additional Skills &amp; Qualifications</strong></p><p>New York State licensed RN. </p><p>Bachelor&#39;s degree required. 2-5 years minimum clinical experience. </p><p>Proficient in phlebotomy, basic clinical assessments, IV skills</p><p>Follow a detailed clinical research protocol. </p><p>Excellent organizational skills, problem solving and communication skills required.</p><p><strong>Experience Level</strong></p><p>Intermediate Level</p>

Clinical Research Nurse - Entry Level

<h1><strong>Job Title: Clinical Research Nurse - Oncology</strong></h1><p><br></p><h2>Job Description</h2><p>The Clinical Research Coordinator II RN is responsible for planning, coordinating, evaluating, and performing nursing care for participants in assigned research projects. This role involves adhering to study protocols, FDA regulations, and ICH/GCP guidelines while advocating for patient safety and rights.</p><p><br></p><h2>Responsibilities</h2><ul><li>Deliver safe care and demonstrate regard for the dignity and respect of all participants.</li><li>Maintain clinical competencies including physical assessment, phlebotomy, and IV insertion.</li><li>Practice Universal Precautions and abide by HIPAA regulations.</li><li>Maintain a clean and prepared clinical space, performing set-up and turnover procedures.</li><li>Participate in training programs to maintain licensure.</li><li>Utilize positive interpersonal communication skills with healthcare team members, patients, investigators, and sponsors.</li><li>Review informed consent documents with study candidates to ensure patient rights and safety.</li><li>Manage multiple clinical trial protocols, coordinating execution and follow-up, and performing accurate documentation.</li><li>Promote Principal Investigator oversight by advising on deviations and patient status.</li><li>Coordinate the work of support staff, laboratory technicians, and assistants to ensure adherence to research protocols.</li></ul><h2> Qualifications</h2><ul><li>Ability to perform clinical tasks and assist with minor procedures.</li><li>Ability to integrate into various clinical settings as needed.</li><li>Skills in physical assessment, phlebotomy, and IV insertion.</li><li>Associate degree in Nursing.</li><li>Minimum 2 years of Clinical Research experience.</li><li>3+ years oncology experience </li><li>Current, active State of FL license as a Registered Nurse.</li><li>Basic Life Support (BLS) certification.</li></ul><h2>Work Environment</h2><p>The position is based in a hospital setting, requiring interaction with various clinical teams and adherence to hospital protocols.</p>

Clinical Research Nurse - Oncology

<p style="text-align: center;"><strong>Clinical Research Nurse Director</strong></p><p style="text-align: center;">The Clinical Research Nurse Director will be responsible for managing all aspects of clinical research operations, ensuring regulatory compliance, and</p><p style="text-align: center;">delivering high-quality patient care. This role involves collaboration with the CEO, Principal Investigators, and Sub-Investigators, and includes the supervision of one Clinical Research Nurse (CRN) to start.</p><p><strong><u>Key Responsibilities</u></strong></p><p><strong>Clinical Oversight </strong>– Screen and prepare patients, assist physicians,manage medications, and ensure patient safety during study procedures</p><p><strong>Study Management</strong>– Maintain study documentation, drug accountability, and oversee monitoring visits</p><p><strong>Administrative Duties </strong>– Develop SOPs, manage contracts, prepare regulatory submissions, and support audits</p><p><strong>Coordination </strong>– Liaise with pharmaceutical sponsors, service providers,and referring physicians</p><p><strong>Personnel Management </strong>–Supervise and support research staff</p><p><strong>Financial Oversight </strong>– Monitor payments, manage invoicing, and ensure financial accuracy</p><p><br></p><p><strong><u>Qualifications</u></strong></p><p>Registered Nurse (Georgia license required)</p><p>Minimum 5 years of clinical research experience</p><p>At least 3 years in a site management or director-level role in a research setting</p><p>Clinical research management and coordination</p><p>Regulatory compliance,including FDA submissions, GCP, SOP, and IRB</p><p>Phlebotomy and infusion skills</p><p>Experience in managing budgets and contracts</p>

Clinical Research Nurse Director

<h3>&#128138; Clinical Review Pharmacist – <strong>100% Remote</strong></h3><p><strong>$55/hr | Full-Time | Contract-to-Hire | Make a Real Impact from Anywhere</strong></p><p><br></p><p><strong>&#128640; Why This Role Rocks</strong>  </p><p>Join a team of pharmacy professionals making real-time decisions that directly impact patient care. In this fully remote role, you’ll use your clinical expertise to review and approve (or deny) requests like prior authorizations, formulary exceptions, and quantity limit overrides—all while collaborating with a knowledgeable and supportive team. If you&#39;re detail-driven, passionate about clinical outcomes, and enjoy autonomy with purpose, this is your kind of opportunity.</p><p>Contracts are reviewed every six months, and pharmacists here are routinely considered for long-term roles after 18–24 months.</p><p><br></p><p><strong>What You&#39;ll Do</strong></p><ul><li>Conduct independent reviews of utilization management requests</li><li>Assess coverage requests with client-specific clinical criteria</li><li>Meet monthly targets for quality and productivity</li><li>Collaborate with pharmacy peers and clinicians</li><li>Engage in provider and member communication if trained for call center counseling</li></ul><p><strong>Training &amp; Schedule Highlights</strong></p><ul><li><strong>Training:</strong> ~16 weeks | Monday–Friday | 8:00 AM – 4:30 PM CST<ul><li>Includes live instruction, interactive materials, and hands-on practice audits</li><li><strong>Heads-up:</strong> No time off during training (barring rare exceptions)</li></ul></li><li><strong>Schedule After Training:</strong><ul><li>8-hour shifts starting at 9:00 or 10:00 AM CST</li><li>Assigned via team bidding based on seniority</li><li>Expect overtime during peak season (Nov–May)</li><li>Rotating weekends and holidays—bid-based scheduling ensures fairness</li></ul></li></ul><p><strong>Logistics &amp; Perks</strong></p><ul><li>Up to <strong>120 hours of unpaid time off annually</strong>, depending on seniority</li><li>6+ month initial contract with strong potential to convert to long-term</li><li>Projected start dates: <strong>September–October</strong></li><li><strong>100% Remote – Work from anywhere</strong> (except CA, HI, or VA)</li><li>Must hold an active pharmacist license in good standing in any other U.S. state</li></ul><p><strong>Ideal Candidate Profile</strong></p><ul><li>PharmD or Bachelor’s in Pharmacy</li><li>At least 2 years of experience in retail, managed care, or clinical pharmacy</li><li>Solid decision-making skills with a knack for details and communication</li><li>Looking for meaningful, long-term impact while working remotely</li></ul>

Clinical Review Pharmacist - Remote

<h1 style="font-weight: 700;">Job Title: <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span></span></span></span></span></span></span> Clinical Project Manager</h1><br><h2>Job Description</h2><p>We are seeking a dedicated <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span></span></span></span></span></span></span> Clinical Project Manager responsible for overseeing the planning, execution, and management of clinical trials across multiple phases. This role ensures compliance with regulatory requirements, timelines, and budget constraints while driving operational excellence in clinical trial execution.</p><br><h2>Responsibilities</h2><ul><li>Lead end-to-end clinical trial management from protocol development to study closeout.</li><li>Develop and maintain detailed project plans, timelines, and budgets.</li><li>Collaborate with regulatory teams for submissions, amendments, and compliance-related documentation.</li><li>Address protocol deviations, audit findings, and inspection readiness.</li><li>Select, negotiate, and manage relationships with CROs, central labs, and other external vendors.</li><li>Track performance metrics and ensure service level agreements are met.</li><li>Proactively identify study risks and develop mitigation strategies.</li><li>Address operational challenges, protocol deviations, and recruitment/retention issues.</li><li>Ensure efficient resource allocation to optimize study costs.</li><li>Monitor trial-related invoices and payments in collaboration with finance teams.</li><li>Act as the primary point of contact for all internal and external stakeholders.</li><li>Provide leadership and mentorship to junior project managers, CRAs, and study coordinators.</li><li>Facilitate collaboration among cross-functional teams including Clinical Operations, Data Management, Medical Writing, Quality Assurance, and other departments.</li><li>Ensure high-quality data collection and adherence to data integrity standards.</li><li>Work closely with data management and biostatistics teams to ensure timely database locks.</li><li>Provide regular study updates to <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">senior</span></span></span></span></span></span></span></span></span> leadership and stakeholders.</li><li>Develop strategies to optimize patient recruitment and retention.</li><li>Oversee site relationships, investigator engagement, and performance metrics.</li><li>Support protocol development and feasibility assessments.</li><li>Contribute to clinical development plans, study endpoints, and operational feasibility considerations.</li><li>Develop organizational systems including SOPs, document management systems, and project finance management.</li><li>Ensure compliance with regulatory requirements and standard operating procedures.</li><li>Perform any other duties as assigned by the supervisor.</li></ul><h2>Essential Skills</h2><ul><li>Strong leadership, communication, and negotiation skills.</li><li>Ability to work in a fast-paced environment and manage multiple priorities.</li><li>Proficiency in clinical trial management systems (CTMS) and regulatory submission platforms.</li><li>Excellent problem-solving and risk management abilities.</li><li>Financial acumen for budget forecasting and cost control.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in life sciences, pharmacy, nursing, or a related field (Master’s or PhD preferred).</li><li>7+ years of experience in clinical trial management within the pharmaceutical, biotech, or CRO industry.</li><li>Proven experience in leading Phase I-IV clinical trials.</li><li>Strong understanding of GCP, ICH guidelines, FDA, EMA, and other regulatory requirements.</li><li>Experience managing CROs, vendors, and multi-site global trials.</li><li>Prior experience in neurology and rare diseases is a plus.</li><li>Experience working in an FDA-regulated and/or EMA-regulated environment.</li><li>Knowledge of adaptive trial designs and decentralized clinical trials is an advantage.</li></ul><h2>Work Environment</h2><p>This position will require domestic and international travel (10%). The work environment is dynamic and performance-driven, offering high visibility in a smaller company setting. The company provides a supportive culture with a rewards program, cellphone reimbursement, tuition reimbursement, 401K matching, and excellent benefits. Employees are encouraged to take ownership of tasks and proactively seek solutions, working in a collaborative and goal-oriented environment.</p><br>

Clinical Trial Manager

<h1 style="font-weight: 700;">Job Title: <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span></span></span></span></span></span> Clinical Project Manager</h1><br><h2>Job Description</h2><p>We are seeking a dedicated <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span></span></span></span></span></span> Clinical Project Manager responsible for overseeing the planning, execution, and management of clinical trials across multiple phases. This role ensures compliance with regulatory requirements, timelines, and budget constraints while driving operational excellence in clinical trial execution.</p><br><h2>Responsibilities</h2><ul><li>Lead end-to-end clinical trial management from protocol development to study closeout.</li><li>Develop and maintain detailed project plans, timelines, and budgets.</li><li>Collaborate with regulatory teams for submissions, amendments, and compliance-related documentation.</li><li>Address protocol deviations, audit findings, and inspection readiness.</li><li>Select, negotiate, and manage relationships with CROs, central labs, and other external vendors.</li><li>Track performance metrics and ensure service level agreements are met.</li><li>Proactively identify study risks and develop mitigation strategies.</li><li>Address operational challenges, protocol deviations, and recruitment/retention issues.</li><li>Ensure efficient resource allocation to optimize study costs.</li><li>Monitor trial-related invoices and payments in collaboration with finance teams.</li><li>Act as the primary point of contact for all internal and external stakeholders.</li><li>Provide leadership and mentorship to junior project managers, CRAs, and study coordinators.</li><li>Facilitate collaboration among cross-functional teams including Clinical Operations, Data Management, Medical Writing, Quality Assurance, and other departments.</li><li>Ensure high-quality data collection and adherence to data integrity standards.</li><li>Work closely with data management and biostatistics teams to ensure timely database locks.</li><li>Provide regular study updates to <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">senior</span></span></span></span></span></span></span></span> leadership and stakeholders.</li><li>Develop strategies to optimize patient recruitment and retention.</li><li>Oversee site relationships, investigator engagement, and performance metrics.</li><li>Support protocol development and feasibility assessments.</li><li>Contribute to clinical development plans, study endpoints, and operational feasibility considerations.</li><li>Develop organizational systems including SOPs, document management systems, and project finance management.</li><li>Ensure compliance with regulatory requirements and standard operating procedures.</li><li>Perform any other duties as assigned by the supervisor.</li></ul><h2>Essential Skills</h2><ul><li>Strong leadership, communication, and negotiation skills.</li><li>Ability to work in a fast-paced environment and manage multiple priorities.</li><li>Proficiency in clinical trial management systems (CTMS) and regulatory submission platforms.</li><li>Excellent problem-solving and risk management abilities.</li><li>Financial acumen for budget forecasting and cost control.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in life sciences, pharmacy, nursing, or a related field (Master’s or PhD preferred).</li><li>7+ years of experience in clinical trial management within the pharmaceutical, biotech, or CRO industry.</li><li>Proven experience in leading Phase I-IV clinical trials.</li><li>Strong understanding of GCP, ICH guidelines, FDA, EMA, and other regulatory requirements.</li><li>Experience managing CROs, vendors, and multi-site global trials.</li><li>Prior experience in neurology and rare diseases is a plus.</li><li>Experience working in an FDA-regulated and/or EMA-regulated environment.</li><li>Knowledge of adaptive trial designs and decentralized clinical trials is an advantage.</li></ul><h2>Work Environment</h2><p>This position will require domestic and international travel (10%). The work environment is dynamic and performance-driven, offering high visibility in a smaller company setting. The company provides a supportive culture with a rewards program, cellphone reimbursement, tuition reimbursement, 401K matching, and excellent benefits. Employees are encouraged to take ownership of tasks and proactively seek solutions, working in a collaborative and goal-oriented environment.</p><br>

<p style="text-align: center;"><strong><u>Urgent Hiring for Pharmacist in Tulsa ,OK</u></strong></p><p style="text-align: center;"><strong><u>﻿*Must be located closer to Tulsa ,OK*</u></strong></p><p style="text-align: center;"><br></p><p><strong><u>Job Description:</u></strong></p><ul><li>Monitor drug therapy regimens for contraindications, drug-drug interactions, drug-food interactions, allergies, and appropriateness of drug and dose.</li><li>Provide accurate and timely medication information to healthcare staff and patients.</li><li>Interact proactively with medical staff regarding drug therapy issues.</li><li>Document all clinical activities and interventions accurately and completely.</li></ul><p><strong><u>Qualifications: </u></strong></p><ul><li><strong>B.S. or Pharm D. from an ACPE-accredited School of Pharmacy is Mandatory</strong></li><li><strong>Active Pharmacist license in Oklahoma State Board of Pharmacy is Mandatory</strong></li><li><strong>1+ year of hospital pharmacy experience is Mandatory</strong></li></ul><p><strong>BLS &amp; ACLS certification is Preferred</strong></p>

Clinical/ER/NICU Pharmacist

<h1 style="font-weight: 700;">Job Title: Programmer</h1><br><h2>Job Description</h2><p>This role requires a strong understanding of Geometric Dimensioning and Tolerancing (GD&amp;T) to perform inspections using Coordinate Measuring Machines (CMM). The successful candidate will create, debug, and verify CMM programs using VeriSurf software while collaborating with customers to ensure program alignment. You will be responsible for conducting AS9102 First Article Inspections (FAI) and generating corresponding reports, as well as providing feedback to the program management team regarding labor hours required for CMM inspections. Additionally, you will work closely with the Program Management team to provide inspection quotes and lead times.</p><br><h2>Responsibilities</h2><ul><li>Perform inspections using CMM and create, debug, and verify CMM programs running VeriSurf software.</li><li>Collaborate with customers for alignment on CMM programs.</li><li>Conduct AS9102 FAI inspections and generate corresponding reports.</li><li>Provide feedback to program management team for labor hours to perform a CMM inspection.</li><li>Work alongside Program Management team to provide inspection quotes and lead times.</li><li>Utilize strong knowledge of inspection tools such as gauges and calipers.</li><li>Communicate closely with production managers and program managers to resolve immediate issues.</li><li>Approve final inspection products to meet specified requirements.</li><li>Deliver inspection results to Program Managers and other departments as necessary.</li><li>Document inspection results using internal QA database, FAIRs, AS9102 FAIR, PPAP reports.</li><li>Document Non-Conforming Material/RMAs.</li><li>Follow guidelines for using and maintaining measurement tools.</li><li>Provide feedback to the QA Manager for any inspection issues.</li></ul><h2>Essential Skills</h2><ul><li>Strong knowledge of GD&amp;T.</li><li>Experience with CMM programming and VeriSurf software.</li><li>Ability to read, write, communicate, and comprehend basic instructions.</li><li>Experience with inspection tools such as calipers, height gauges, micrometers.</li><li>Knowledge of ISO9001/AS9100D Standard.</li><li>Proficiency in Microsoft Excel, Word, and PowerPoint.</li><li>Attention to detail and excellent verbal and written communication skills.</li><li>Ability to work independently and read drawings and understand symbols.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High School Diploma at minimum with 4 years of related experience or equivalent combination of education and experience.</li><li>Previous experience using CMM or articulating arms.</li><li>Experience using VeriSurf CMM software is a plus.</li><li>Knowledge of FMEAs, corrective actions, and QMS systems.</li></ul><h2>Work Environment</h2><p>The work schedule is from 8am to 5pm. You will be part of a team consisting of 9 inspectors, 1 document control, and 1 supervisor.</p><br>

Cmm Programmer

<p><strong>Description</strong></p>
					<p>We are seeking an experienced CNC Programmer with expertise in MazaCAM programming for Mazak QTE-300M SG and Mazak QT-450M machines. The ideal candidate will have strong programming skills, hands-on machining experience, and the ability to optimize processes for efficiency and precision.</p>
					<p><strong>Skills</strong></p>
					<p>cnc programming, cnc machining, lathe setup, lathe programming, lathe operation, mazak lathe, cad/cam</p>
					<p><strong>Top Skills Details</strong></p>
					<p>cnc programming,cnc machining,lathe setup,lathe programming,lathe operation,mazak lathe,cad/cam</p>
					<p><strong>Additional Skills &amp; Qualifications</strong></p>
					<p>•	Proven experience in CNC programming with MazaCAM for Mazak QTE-300M SG and Mazak QT-450M.
•	Strong knowledge of GD&amp;T.
•	Strong knowledge of Mazak controls, tooling, and machining best practices.
•	Ability to read and interpret blueprints, GD&amp;T, and technical drawings.
•	Experience with CNC lathe setup, troubleshooting, and process optimization.
•	Willingness and ability to travel to Italy one week per month.
•	Strong problem-solving skills and attention to detail.
•	Ability to work independently and within a team environment.</p>
					<p><strong>Experience Level</strong></p>
					<p>Intermediate Level</p>

Cnc Machinist And Programmer

<h1 style="font-weight: 700;">Job Title: Programmer</h1><br><h2>Job Description</h2><p>We are seeking a skilled programmer proficient in utilizing the latest SolidWorks 3D solid modeling software for fixture and tooling design. The ideal candidate will have a foundational understanding of GD &amp; T and the ability to create or modify CNC programs for manufacturing purposes. This role involves supporting the development and introduction of new products into manufacturing, developing routings using the current ERP system, and designing work holding and cutting tool technology to enhance machine performance.</p><br><h2>Responsibilities</h2><ul><li>Utilize SolidWorks 3D solid modeling software for fixture and tooling design.</li><li>Create or modify CNC programs for manufacturing processes.</li><li>Support the development and introduction of new products into manufacturing.</li><li>Develop routings using the current ERP system.</li><li>Design work holding and cutting tool technology to improve machine performance.</li><li>Provide support in developing new CNC machine tool requirements.</li><li>Work closely with operators and engineers to troubleshoot CNC programs and machining operations.</li><li>Support new capital projects.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in SolidWorks and/or MasterCAM.</li><li>Experience in machining and fabrication.</li><li>2+ years of experience with a 2-year degree in Engineering or similar, or 5+ years with no degree.</li><li>Ability to utilize Microsoft Office programs such as Word and Excel.</li><li>Proficiency with the latest Mastercam CAM software for CNC program creation and verification.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Self-starter with the ability and desire to continuously improve skills.</li></ul><h2>Work Environment</h2><p>This position is for the 2nd shift with working hours from 3 PM to 1 AM or 1 PM to 11 PM, Monday through Thursday. The role reports to the ME and Engineering Manager.</p><br>

Cnc Programmer

<h1><strong>Job Title: CNC Programmer</strong></h1><p><br></p><h2>Job Description</h2><p>The CNC Programmer will be responsible for writing machining programs using Mastercam CAM software. This role involves providing technical expertise and support to the production floor, as well as creating process documentation for the planning department, including set-up sheets, perishable tooling, and in-process inspection requirements. The programmer will also investigate process problems affecting manufacturing and quality assurance and recommend improvements to enhance performance, increase reliability, and reduce costs.</p><p><br></p><h2>Responsibilities</h2><ul><li>Write machining programs using Mastercam CAM software.</li><li>Provide technical expertise and support to the production floor.</li><li>Create process documentation for the planning department, including set-up sheets, perishable tooling, and in-process inspection requirements.</li><li>Investigate process problems affecting manufacturing and quality assurance.</li><li>Recommend improvements to manufacturing processes to improve performance, increase reliability, and decrease cost.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in CNC mill operations.</li><li>Expertise in Mastercam software.</li><li>Knowledge of GD&amp;T and CNC programming.</li><li>Minimum of 10 years of experience in programming multi-axis CNC mills in a manufacturing environment.</li><li>At least 5 years of experience in the aerospace industry.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience machining materials such as aluminum, stainless steel, titanium, and alloy steels.</li><li>Familiarity with ISO 9001 and/or AS9100 quality systems and documentation.</li></ul><h2>Work Environment</h2><p>The work environment involves machining high-performance engine components for various industries, including motorsports, aerospace, defense, space, medical, and other high-tech sectors. The team consists of five programmers, each supporting their own machines. </p>

<h1><strong>Job Title: CNC Programmer</strong></h1><p><strong>Irving, TX</strong></p><p><br></p><h2>Job Description</h2><p>We are seeking an experienced CNC Programmer to become an integral part of our fabrication team. This role is centered around creating precise CNC programs for laser cutting, punching, tube laser, and bending machines using Trumpf TruTops Boost. The ideal candidate will excel in reading engineering drawings, selecting appropriate tooling, and determining optimal bend sequences. A comprehensive understanding of sheet metal fabrication processes and material optimization is crucial. You will collaborate closely with engineers and operators to troubleshoot issues, enhance workflow, and support production efficiency in a dynamic environment.</p><p><br></p><h2>Responsibilities</h2><ul><li>Utilize Trumpf TruTops Boost to calculate bend deductions and create flat patterns for accurate preparation of parts for punch, lasers, and press brakes.</li><li>Develop CNC programs for laser cutting, punching, tube laser, and bending machines using Trumpf TruTops Boost.</li><li>Select appropriate tooling based on material type and thickness.</li><li>Determine proper brake tooling and bend sequences.</li><li>Read and interpret engineering drawings and work orders.</li><li>Collaborate with team members to optimize productivity.</li><li>Demonstrate strong attention to detail and ability to follow instructions accurately.</li><li>Troubleshoot issues related to CAD/CAM outputs, nesting errors, and machine compatibility.</li><li>Complete work accurately and in a timely manner with attention to detail.</li></ul><h2>Essential Skills</h2><ul><li>2+ years experience in sheet metal fabrication operations such as experience in Punch, Laser, Panel Bender, Tube Laser, Brake Press.</li><li>2+ years of experience with programming sheet metal fabrication machines using Trumpf TruTops Boost software (preferred) or similar CNC software.</li><li>Familiarity with MRP/ERP software for fabrication workflows.</li><li>Demonstrated ability to read blueprints and develop optimal tool paths and setups with high accuracy and attention to maximum material utilization.</li><li>Excellent oral and written communication skills.</li><li>Ability to multi-task in a fast-paced team-oriented manufacturing environment.</li><li>Strong problem-solving skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Nesting experience is a plus.</li></ul><h2>Work Environment</h2><p>The position is based in an office environment with scheduled time on the factory floor for collaboration meetings. The role is expected to work 40 hours per week, with flexible start time schedules available.</p>

<h1><strong>Job Title: CNC Programmer</strong></h1><p><br></p><h2>Job Description</h2><p>As a CNC Programmer, you will be responsible for creating and editing 2D and 3D CNC programs for the fabrication of models and other components. You will debug and optimize CNC programs to ensure accuracy and performance, set up and run CNC machines, and make improvements as needed. Utilizing CAD/CAM software, you will adjust designs for shrinkage and material loss during part production, maintain accurate documentation, and assist with troubleshooting technical issues. You will also read and interpret blueprints, sketches, and verbal instructions.</p><p><br></p><h2>Responsibilities</h2><ul><li>Create and edit 2D and 3D CNC programs for model fabrication.</li><li>Debug and optimize CNC programs for accuracy and performance.</li><li>Set up and run CNC machines, checking performance and making improvements.</li><li>Utilize CAD/CAM software to adjust designs for shrinkage and material loss.</li><li>Maintain accurate documentation of all programming activities.</li><li>Assist in troubleshooting and resolving technical issues.</li><li>Read and interpret blueprints, sketches, and verbal instructions.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in CNC programming, including CNC mill and lathe operations.</li><li>Experience with Solidworks and familiarity with PDM vault.</li><li>Proficiency in HyperMILL programming.</li><li>Ability to program for at least 3-axis CNC machines.</li><li>Experience in a shop environment for a minimum of 3 years.</li><li>Technical college degree in a related field.</li><li>Solid mathematical skills and problem-solving abilities.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>TIG welding experience.</li><li>Experience with 5-axis programming.</li><li>Blueprint reading and interpretation.</li><li>Experience with MasterCAM programming.</li></ul><h2>Work Environment</h2><p>You will work in a clean, well-maintained facility equipped with state-of-the-art equipment. The work schedule primarily involves the first shift, starting between 5-6 AM, with up to 10 hours of overtime weekly. The environment encourages automation and aims to move away from manual post-processing. Profit sharing is available with a 15% annual payout, and there is potential for career advancement into tooling engineering. The culture is strong, with low attrition rates and opportunities for training in advanced programming skills. </p>

<h1 style="font-weight: 700;">Job Title: Color Laboratory Technician</h1><br><h2>Job Description</h2><p>We are seeking a skilled Color Laboratory Technician to join our team. This role requires expertise in color matching, formulating, and designing various resins, including olefins, engineering resins, glass-filled, and high-heat resins. The ideal candidate will have prior experience in a color house, with a preference for those with pellet master batch formulation experience. Candidates with liquid color formulation experience may also be considered with additional training.</p><br><h2>Responsibilities</h2><ul><li>Match colors accurately and formulate designs for various resins.</li><li>Perform quality control and quality assurance tasks.</li><li>Conduct laboratory tests and inspections to ensure high standards.</li><li>Collaborate with production, sales, and customer service teams.</li><li>Operate small-scale molding machines and weigh small amounts of pigments.</li><li>Work independently while effectively contributing to team efforts.</li></ul><h2>Essential Skills</h2><ul><li>Expertise in color matching and chemistry.</li><li>Basic math skills.</li><li>Ability to pass a color test.</li><li>Operation of small-scale molding machines.</li><li>Quality control and quality assurance experience.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>College-level education in polymer science and color theory is preferred.</li><li>Minimum of 2 years of experience, but 1 year may be considered for a strong candidate.</li><li>Experience in extrusion and screen printing is beneficial.</li></ul><h2>Work Environment</h2><p>The position is based in a laboratory setting. The working hours are from 6 AM to 4:30 PM, Monday through Friday, with occasional overtime as needed.</p><br>

Color Laboratory Technician

<h1 style="font-weight: 700;">Job Title: Systems Technician</h1><br><h2>Job Description</h2><p>We are seeking a skilled Systems Technician to join a team dedicated to Combat System Integration support for Non-AEGIS class ships. The role requires expertise in Radar and Ship Self Defense Systems (SSDS), supporting physical design, installation, testing, and maintenance of US Navy Combat Systems.</p><br><h2>Responsibilities</h2><ul><li>Actively participate as part of a team of engineers, technicians, and support personnel to provide ship integration services.</li><li>Perform technical reviews of planned ship upgrades, coordinating Ship Integration Liaison Action Reports (LARs), and provide written comments on issues and impacts.</li><li>Generate and conduct technical reviews of Combat Systems Integration/Engineering Ship Change Documents (SCDs).</li><li>Review Combat Systems changes to identify possible conjunctive alteration impacts with other ship systems.</li><li>Participate in assessment events related to integration and testing of ship systems.</li><li>Conduct Ship Checks to document existing compartment arrangements and configurations.</li></ul><h2>Essential Skills</h2><ul><li>10+ years of experience as either a Fire Control Technician (FC) or Electronics Technician (ET) or 5 years of experience in ship system engineering support.</li><li>Specific experience in Ship Self Defense Systems and/or Radar Systems.</li><li>Familiarity with ship system design processes including SCDs, ECPs, and ECRs.</li><li>Familiarity with US Navy Ship Specification Documents such as GSO, Ship Specs, and MIL-STDs.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Recent experience supporting NSWCDD.</li><li>Experience with AutoCAD.</li></ul><h2>Work Environment</h2><p>The work is primarily onsite with potential for hybrid flexibility once up to speed. This role offers the opportunity to work on Non-AEGIS ships including amphibious submersibles and Aircraft Carriers, contributing to the safety and modernization of naval technologies.</p><br>

Combat Systems Technician

<p><strong>Description</strong></p>
					<p>This Client is seeking commissioning engineer with a mechanical <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">background</span></span> that has experience within datacenters markets and able to help carry out project assignments.
  Experience working within the following vertical markets:  Hospitals, Large / Complex Facilities and Mission Critical Facilities (data centers, telecommunications, or disaster recovery sites)
  Participate in daily commissioning activity meetings which services include:
•       Equipment pre-start-up procedures; Development of standard operating procedures (SOP&#39;s) and Methods of Procedures (MOPs); Comprehensive Commissioning documentation;
•       Prepare commissioning test procedures and reports
•       Develop and maintain commissioning logs, equipment checklist, and other tools to track commissioning projects
•       Write comprehensive reports which include the following sections: recommendations for optimizing building operations, functional checklists, list of deficiencies, equipment operation and maintenance manuals
•       Review design criteria, specifications, drawings, equipment submittals, and other documentation pertinent to commissioning
•       Develop and administer functional tests for various systems, such as mechanical central chilled water plants, packaged rooftop units, boilers, chillers, computer room air conditioning units, fire protection systems, etc. 
•       Integrated system testing; Building management system testing; Compilation of all testing procedure results</p>
					<p><strong>Skills</strong></p>
					<p>Construction, Commissioning, Control system, Engineering, mechanical design, mechanical engineering, mechanical equipment</p>
					<p><strong>Top Skills Details</strong></p>
					<p>Construction,Commissioning</p>
					<p><strong>Additional Skills &amp; Qualifications</strong></p>
					<p>  Minimum 10 years’ experience in the Electrical Mission Critical Field
  Bachelor&#39;s / Associates Degree as an Mechanical Engineer a plus
  A/E experience working in complex facilities or mission-critical projects a big plus
  Good communication skills, Interface with clients, contractors, equipment vendors, and owners agents as needed; Execute project assignments; Interface with project contractors, vendors, and testing technicians; Interact with all facets of the company: engineering, design, etc
  Experience with IEEE procedures and protocols a plus
  Possess basic knowledge of system design
  Commissioning certification or PE
  OSHA 10/30 certification a plus</p>
					<p><strong>Experience Level</strong></p>
					<p>Intermediate Level</p>

Commissioning Engineer

<p><br></p><h2>Essential Skills</h2><ul><li>2+ years of experience in commissioning or construction for I&amp;C or Electrical Basebuild systems in the Advanced Technology sector.</li><li>Experience with Rockwell Automation, PLC5, and Control Logix hardware and software.</li><li>Experience with multi-discipline large capital projects involving Owners, General Contractors, Contractors, and System Integrators.</li><li>Good understanding of Design/Build (Engineering and Construction).</li><li>Knowledge of complex process systems architecture &amp; design, Instrumentation, Device Selection, Networking, PLC &amp; I/O architectures, P&amp;IDs, data sheets, and SCADA.</li><li>Working knowledge of environments common in large industrial applications such as Dry/Wet Mechanical, AWN, Gas/Chem Distribution, HVAC, and Clean Room environmental control.</li><li>Proficient in written and verbal technical communication including generating reports and conducting group presentations.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in electrical, mechanical, chemical engineering or similar technical field (preferred).</li><li>Associate&#39;s degree or technical certification in electrical, mechanical, or control systems engineering or a related field. Direct experience will be considered in lieu of degree.</li><li>Minimum of 3 years of experience working with control systems in a data center or similar environment.</li><li>Proficiency in control systems programming and configuration.</li><li>Strong understanding of HVAC, electrical, and building automation systems.</li><li>Ability to read and interpret technical drawings and schematics.</li><li>Familiarity with various control system platforms; BMS or SCADA is a plus.</li><li>Experience conducting I/O checkouts.</li><li>Excellent problem-solving and analytical skills.</li><li>Strong communication and teamwork abilities.</li><li>Attention to detail and a proactive approach to work.</li></ul><h2>Work Environment</h2><p>The role is onsite in Abilene and includes a per diem. The working hours are 50 hours per week.</p>

Commissioning Engineering Technician

<p><br></p><h2>Essential Skills</h2><ul><li>2+ years of experience in commissioning or construction for I&amp;C or Electrical Basebuild systems in the Advanced Technology sector.</li><li>Experience with Rockwell Automation, PLC5, and Control Logix hardware and software.</li><li>Experience with multi-discipline large capital projects involving Owners, General Contractors, Contractors, and System Integrators.</li><li>Good understanding of Design/Build (Engineering and Construction).</li><li>Knowledge of complex process systems architecture &amp; design, Instrumentation, Device Selection, Networking, PLC &amp; I/O architectures, P&amp;IDs, data sheets, and SCADA.</li><li>Working knowledge of environments common in large industrial applications such as Dry/Wet Mechanical, AWN, Gas/Chem Distribution, HVAC, and Clean Room environmental control.</li><li>Proficient in written and verbal technical communication including generating reports and conducting group presentations.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in electrical, mechanical, chemical engineering or similar technical field (preferred).</li><li>Associate&#39;s degree or technical certification in electrical, mechanical, or control systems engineering or a related field. Direct experience will be considered in lieu of degree.</li><li>Minimum of 3 years of experience working with control systems in a data center or similar environment.</li><li>Proficiency in control systems programming and configuration.</li><li>Strong understanding of HVAC, electrical, and building automation systems.</li><li>Ability to read and interpret technical drawings and schematics.</li><li>Familiarity with various control system platforms; BMS or SCADA is a plus.</li><li>Experience conducting I/O checkouts.</li><li>Excellent problem-solving and analytical skills.</li><li>Strong communication and teamwork abilities.</li><li>Attention to detail and a proactive approach to work.</li></ul><h2>Work Environment</h2><p>The role is onsite in South Bend , IN . Normal work week, M- F Weekends off </p>

Commissioning Engineering Technician-  PLC

<p style="text-align: center;"><strong>*If interested in this role, please contact Kyle McLean at kymclean@actalentservices.com*</strong></p><p style="text-align: center;"><br></p><h2><strong>Commissioning Controls Technician - Abilene TX (If you are not local, per diem is included)</strong></h2><p>Overview:</p><h3>Seeking a detail-oriented Commissioning Engineer to support scheduling, quality assurance, and system integration for Basebuild utility systems. This role involves coordinating commissioning activities, troubleshooting system issues, and interfacing with design and construction teams.</h3><h3>Key Responsibilities:</h3><ul><li>Coordinate technician schedules and manpower forecasts</li><li>Track and resolve commissioning constraints and deficiencies</li><li>Integrate construction/design schedules with commissioning timelines</li><li>Conduct system walkdowns and root cause failure analysis</li><li>Train and manage supplier access in commissioning software</li><li>Generate reports on schedule and quality metrics</li><li>Collaborate with engineering teams and client representatives</li></ul><hr><h3>Qualifications:</h3><ul><li>2+ years in commissioning or construction (I&amp;C or Electrical systems)</li><li>Experience with Rockwell Automation, PLC5, and Control Logix</li><li>Familiarity with large capital projects and multi-discipline teams</li><li>Strong understanding of process systems, P&amp;IDs, SCADA, and BMS</li><li>Proficient in reading technical drawings and conducting I/O checkouts</li><li>Excellent communication, problem-solving, and teamwork skills</li></ul><hr><h3>Preferred:</h3><ul><li>Bachelor’s or Associate’s degree in engineering or related field</li><li>3+ years working with control systems in data centers or similar environments</li></ul><p> </p>

Commissioning Engineering Techs

<h1 style="font-weight: 700;">Job Title: Commissioning Manager</h1><br><h2>Job Description</h2><p>This role requires 100% travel and commitment to one site, primarily new build data centers located mostly in the Southeast. The position involves managing electrical and specialty systems QAQC and commissioning scopes of work, as well as overseeing commissioning and startup schedules.</p><br><h2>Responsibilities</h2><ul><li>Develop and manage QAQC and commissioning scopes, schedules, and budgets.</li><li>Review outgoing QAQC and commissioning estimates with the Estimating Department for accuracy.</li><li>Utilize internal functional groups and monitor progress of project deliverables.</li><li>Develop and implement QAQC and commissioning safety plans in collaboration with internal safety departments.</li><li>Ensure startup and operational procedures are executed safely and comply with client specifications.</li><li>Coordinate daily, weekly, and monthly meetings related to QAQC, commissioning, equipment, coordination, scheduling, staffing, and project management.</li><li>Manage QAQC and commissioning issues logs and coordinate with affected parties to resolve issues.</li><li>Work with third-party testing and commissioning agencies to ensure proper coverage during procedures.</li><li>Collaborate with Human Resources on recruiting, selection, and employee relations.</li><li>Coach and develop managerial talent and effectively select and train individuals.</li><li>Create a supportive environment that encourages learning from mistakes and provides constructive feedback.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in Microsoft Office Suite and Google G-Suite.</li><li>Knowledge of the electrical construction trade.</li><li>Experience in industrial or data center commissioning.</li><li>Bachelor’s Degree in Engineering, Construction Management, or equivalent technical training/experience.</li><li>5 years of experience in Project Management, Construction Management, Project Engineering, or Commissioning Management.</li><li>8 years of experience in commissioning/start-up for electrical and/or mechanical systems.</li><li>Experience leading commissioning/start-up activities for projects exceeding $25MM in contract value.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in Mission Critical, Industrial, and Commercial sectors.</li><li>Experience as an electrician, engineer, technician, or similar role in oil and gas industry.</li></ul><h2>Work Environment</h2><p>The position requires extensive travel and commitment to project sites. A car allowance or rental car/flights are provided. The role involves working with a commissioning team on new build data center projects scattered across various locations, primarily in the Southeast.</p><br>

Commissioning Manager

<p><strong>BESS COMMISSIONING MANAGER</strong></p><p><br></p><p>We are seeking an experienced Commissioning Manager to support <span style="font-family: Calibri, sans-serif; font-size: 11pt;">one of the world’s largest Battery Energy Storage System Developers. The primary roles are to conduct plant testing, performance testing, ISO/GIA/PPA Testing and startup of a Battery Energy Storage System and Solar Coupled Power systems. This role is hybrid between site travel and monthly visits home with per diem offered for on-site travel over 30 days. </span></p><p><br></p><p><strong style="font-family: Calibri, sans-serif; font-size: 11pt;">Responsibilities:</strong></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Participates in safety program and audits</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Support PPA Testing with Customer</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Support GIA Testing with TO</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Support ISO testing</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Manage test energy forecast with the customer</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Support ICCP IT SCADA Team and SCADA PM/Lead with functional checks</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Work with SCADA Integrator and Execution Commissioning Project manager to develop a Commissioning schedule based on Mechanical completion</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Work with SCADA integrator and Commissioning Manger to execute site acceptance testing.</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Support CEWIS Critical Point Checkout with ROCC alarm checks/PGD</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Perform OEM Testing</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Perform Plant Balancing</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Perform Capacity Testing</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Perform notification of AVR/AGC and support</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Review performance data for deficiencies </span></p><p><br></p><p><strong style="font-family: Calibri, sans-serif;">Requirements:</strong></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Battery Energy Storage Systems installation and startup</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Must have a thorough understanding of the technical, performance, and integration of Li-Ion batteries as part of ESS</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Commissioning process creation </span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Understanding of containerized systems, skids, controllers/SCADA, transformers, combiners</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Thorough understanding of DC systems (0-2,000Vdc) and AC systems (480V-34.5kV)</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Experience with control and SCADA systems and troubleshooting</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Organizations skills</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Computer skills MS word, Excel and MS PowerPoint</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Communication to third parties and executives</span></p><p><span style="font-family: Symbol;">·</span><span style="font-size: 7pt;">      </span><span style="font-family: Calibri, sans-serif;">Ability to effectively organize and strategize schedules and plans.</span></p>

<p><strong>Job Title: </strong>Technical Writer – Compliance</p><p><strong>Location: </strong>Parsippany, NJ </p><p><strong>Employment Type: </strong><em>12-Month Contract </em></p><p><strong>Industry: </strong>Pharmaceuticals / Biotechnology</p><hr><h3><strong>About the Role</strong></h3><p>We are seeking a detail-oriented and experienced Technical Writer – Compliance to join our Quality or Manufacturing team. In this role, you will be responsible for authoring, reviewing, and managing investigations and deviations from both compliance and operational perspectives. You will play a key role in ensuring adherence to GMP standards, driving root cause analysis, and supporting continuous improvement initiatives across manufacturing operations.</p><p>This position requires strong technical writing skills, a solid understanding of GMP regulations, and the ability to collaborate effectively with cross-functional teams, including manufacturing personnel and external vendors.</p><hr><h3><strong>Key Responsibilities</strong></h3><ul><li>Lead and author investigations for Deviations, Non-Conformances, OOS/OOT results, field complaints, and environmental excursions.</li><li>Conduct thorough root cause analyses using industry-standard tools and methodologies.</li><li>Develop and implement effective Corrective and Preventive Actions (CAPAs) to prevent recurrence.</li><li>Manage multiple investigations simultaneously, ensuring timely closure in alignment with compliance deadlines and product release schedules.</li><li>Collaborate with cross-functional teams to develop, track, and communicate CAPA plans.</li><li>Identify trends and establish rules to proactively trigger corrective actions.</li><li>Analyze process data to identify opportunities for operational and quality improvements.</li><li>Apply change management principles to support continuous improvement.</li><li>Create and deliver training materials on investigation writing and root cause analysis techniques.</li><li>Serve as a CAPA champion, ensuring timely and effective implementation.</li><li>Maintain clear communication with stakeholders regarding ongoing investigations and CAPAs.</li><li>Ensure all documentation complies with internal quality standards and regulatory requirements.</li></ul><hr><h3><strong>Required Qualifications</strong></h3><ul><li>Bachelor’s degree in a scientific or technical discipline (e.g., Biology, Chemistry, Engineering).</li><li>3–5 years of experience writing and reviewing deviations, investigations, and CAPAs in a GMP-regulated environment.</li><li>Proven experience supporting manufacturing operations in the pharmaceutical, biotechnology, or cell and gene therapy sectors.</li><li>Strong knowledge of aseptic techniques and GMP compliance.</li><li>Proficiency in root cause analysis tools (e.g., 5 Whys, Fishbone, FMEA).</li><li>Excellent technical writing and communication skills.</li><li>Experience working with e-Quality Management Systems (eQMS).</li></ul><hr><h3><strong>Preferred Qualifications</strong></h3><ul><li>Prior experience in Quality Assurance or Compliance roles.</li><li>Familiarity with FDA-regulated operations and regulatory expectations.</li><li>Experience with biologics, cell and gene therapies, or advanced therapy medicinal products (ATMPs).</li><li>Proficiency with Microsoft Office Suite, including Excel, Visio, and Project.</li></ul><hr><h3><strong>Why Join Us?</strong></h3><ul><li>Be part of a mission-driven organization advancing life-saving therapies.</li><li>Collaborate with a passionate and innovative team.</li><li>Opportunity to grow your career in a cutting-edge, fast-paced environment.</li></ul><h1><br></h1>

Compliance Investigator

<h1><strong>Job Title: Compliance Specialist</strong></h1><h1><strong>Pay: 65k+/year </strong></h1><h1><strong>Shift: 1st</strong></h1><p><br></p><h2>Job Description</h2><p>The Compliance Specialist assists in developing, implementing, and monitoring safety programs to reduce the frequency of accidents and injuries, thereby minimizing overall workers’ compensation costs. The role involves working with Tier 2 chemistry and chemical concerns.</p><p><br></p><h2>Responsibilities</h2><ul><li>Plan, implement, communicate, and monitor safety policies and procedures in compliance with local, state, and federal OSHA rules and regulations.</li><li>Audit various elements of safety programs for effectiveness, schedule and perform safety inspections, identify issues, and develop corrective action plans alongside the Director of EHS.</li><li>Supervise, control, and monitor fire prevention and firefighting activities.</li><li>Investigate all accidents and injuries, recommend and/or coordinate corrective actions through root cause analysis completion.</li><li>Lead safety training programs designed to instruct employees in general safe work practices and specific instructions related to job-specific hazards; provide training for new employees.</li><li>Maintain thorough knowledge of federal and state OSHA regulations; keep up-to-date with safety codes and regulations; distribute and/or post new or revised safety standards affecting the company.</li><li>Review and respond to OSHA inquiries in partnership with the Director of EHS.</li><li>Identify potential safety hazards at all facilities, report hazards and recommendations for elimination or reduction to management.</li><li>Assist the Director of EHS in coordinating with other departments on the design and construction of new equipment, facilities, and work methods to ensure compliance with safety policies and regulations.</li><li>Encourage employees and supervisors to report all unsafe conditions immediately and schedule or coordinate repairs promptly.</li><li>Train employees and supervisors to report any injury occurring on the job, even minor ones, immediately.</li><li>Maintain records for statistical measurement and conformance to standard practices of the safety industry.</li><li>Prepare and maintain required safety reports.</li><li>Perform other related duties as assigned by management.</li><li>Knowledge of EHS/LMS system operation.</li></ul><h2>Essential Skills</h2><ul><li>3-5 years of related experience; Bachelor&#39;s degree preferred in Chemistry or Regulatory.</li><li>Experience with storm water and waste water management.</li><li>Knowledge of OSHA regulations and compliance standards.</li><li>Commitment to excellence and high standards.</li><li>Excellent written and oral communication skills.</li><li>Ability to work with all levels of management.</li><li>Strong interpersonal skills.</li><li>Ability to effectively deal with a diversity of individuals at all organizational levels.</li><li>Strong organizational, problem-solving, and analytical skills.</li><li>Proficiency in Word, Excel, Visio, Publisher.</li><li>Ability to manage priorities and workflow.</li><li>Versatility, flexibility, and willingness to work within constantly changing priorities with enthusiasm.</li><li>Good judgment with the ability to make timely and sound decisions.</li><li>Ability to understand all safety requirements and cautions.</li><li>Ability to effectively present information and respond to questions.</li><li>Demonstrated competence in reacting to and handling emergencies.</li><li>Must be able to speak, read, write, and understand the primary language(s) used in the workplace.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bilingual skills are a plus.</li><li>GSP, CSP certifications are a plus.</li><li>First Aid/CPR/AED Trainer certification is a plus.</li><li>OSHA 10/30 Instructor certification is a plus.</li></ul><h2>Work Environment</h2><p>The position requires on-site work in Mentor with 10% domestic travel. The work environment involves engaging with various technologies and systems related to safety management.</p>

Compliance Specialist

<h1 style="text-align: center;"><strong><u>Compliance Specialist</u></strong></h1><p style="text-align: center;"><br></p><p style="text-align: center;">INTERESTED CANDIDATES MAY SEND UPDATED RESUMES TO: JGASSER @ ACTALENTSERVICES.COM </p><p style="text-align: center;">OR TEXT JENNA TO SETUP A PHONE INTERVIEW: 419. 980. 5823</p><p><br></p><p><strong><u>Job Description</u></strong></p><p>As a Safety Specialist, you will assist in developing, implementing, and monitoring safety programs aimed at reducing the frequency of accidents and injuries, while also minimizing overall workers’ compensation costs. You will engage with Tier 2 chemistry and chemical concerns, ensuring a safe workplace for all employees.</p><p><br></p><p><strong><u>Responsibilities</u></strong></p><ul><li>Plan, implement, communicate, and monitor safety policies and procedures in compliance with local, state, and federal OSHA rules and regulations.</li><li>Audit various safety program elements for effectiveness and perform safety inspections to identify issues and develop corrective action plans alongside the Director of EHS.</li><li>Supervise, control, and monitor fire prevention and firefighting activities.</li><li>Investigate all accidents and injuries, recommend corrective actions, and coordinate through root cause analysis completion.</li><li>Lead safety training programs designed to instruct employees in general safe work practices and specific instructions regarding hazards unique to any job assignment, and provide training for new employees.</li><li>Maintain thorough knowledge of federal and state OSHA regulations, safety codes, and regulations, and distribute new or revised safety standards affecting the company.</li><li>Review and respond to OSHA inquiries in partnership with the Director of EHS.</li><li>Identify potential safety hazards at all facilities and report hazards with recommendations for eliminating/reducing to management.</li><li>Coordinate with other departments on the design and construction of new equipment, facilities, and work methods to ensure compliance with safety policies and regulations.</li><li>Encourage employees and supervisors to report all unsafe conditions immediately and schedule or coordinate repairs as soon as possible.</li><li>Train employees and supervisors to report any injury that occurs on the job immediately.</li><li>Maintain records for statistical measurement and conformance to standard practices of the safety industry.</li><li>Prepare and maintain required safety reports.</li><li>Perform other related duties as assigned by management.</li></ul><p><strong><u>Essential Skills</u></strong></p><ul><li>3-5 years of related experience.</li><li>Bachelor&#39;s degree (B.A./B.S.) preferred in Chemistry or Regulatory.</li><li>Experience with stormwater and wastewater management.</li><li>Knowledge of OSHA regulations and compliance standards.</li><li>Proficient in Word, Excel, Visio, and Publisher.</li><li>Ability to manage priorities and workflow.</li><li>Strong organizational, problem-solving, and analytical skills.</li></ul><p><strong><u>Additional Skills &amp; Qualifications</u></strong></p><ul><li>Commitment to excellence and high standards.</li><li>Excellent written and oral communication skills.</li><li>Strong interpersonal skills with the ability to work with all levels of management.</li><li>Ability to deal effectively with a diversity of individuals at all organizational levels.</li><li>Versatility, flexibility, and a willingness to work within constantly changing priorities.</li><li>Good judgement with the ability to make timely and sound decisions.</li><li>Ability to understand safety requirements and cautions.</li><li>Ability to effectively present information and respond to questions.</li><li>Demonstrated competence in reacting to and handling emergencies.</li><li>Must be able to speak, read, write, and understand the primary language used in the workplace.</li><li>Bilingual skills a plus.</li><li>GSP, CSP certification a plus.</li><li>First Aid/CPR/AED Trainer certification a plus.</li><li>OSHA 10/30 Instructor certification a plus.</li></ul><p><strong><u>Work Environment</u></strong></p><p>The role is primarily on-site in Mentor with 10% domestic travel involved. You will be part of a dynamic team, working in an environment that demands high standards of safety compliance and regulatory adherence.</p>

<h1 style="font-weight: 700;">Job Title: Pharmaceutical Compounder</h1><br><h2>Job Description</h2><p>We are seeking a dedicated Pharmaceutical Compounder to join our dynamic Production Department. This role involves working in various areas such as Granulation, Blending, Compression, Coating, Dispensing, or Technical Service, based on project needs and management discretion. Comprehensive training will be provided to ensure proficiency in all assigned tasks.</p><br><h2>Responsibilities</h2><ul><li>Follow all procedures and policies in the manufacturing facility.</li><li>Stay updated with the latest versions of SOPs and document training records.</li><li>Clean, set up, and operate all related equipment in the manufacturing facility.</li><li>Produce pharmaceutical products according to cGMP standards.</li><li>Adhere to Good Documentation Practices.</li><li>Coordinate with the Quality Assurance Department for line clearance after cleaning.</li><li>Work with the Engineering Department or Production Supervisor for equipment or facility breakdowns.</li><li>Train new employees and operators on processing equipment.</li><li>Perform additional tasks as assigned by the Production Supervisor.</li></ul><h2>Essential Skills</h2><ul><li>Experience in Pharmaceutical Compounding, Mixing, Blending, and Compression.</li><li>Pharma GMP experience.</li><li>Proficiency in documentation practices.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High School Graduate or equivalent experience within a pharmaceutical facility.</li><li>Qualified in operating oral solids pharmaceutical manufacturing equipment.</li><li>Basic computer skills, with knowledge of MS Word and Excel being an advantage.</li><li>Strong communication skills for department and inter-departmental coordination.</li><li>Ability to perform basic math and handle stress effectively.</li></ul><h2>Work Environment</h2><p>Join a growing manufacturing department in a new location with stable finances and a family-like environment. Work hours are typically 8-4 or 9-5, with the option to work four 10-hour days. Opportunities for overtime are available during the week or weekends. The role requires accessibility to all areas, safe ladder climbing, wearing required PPE, and the ability to lift up to 100 lbs. You&#39;ll need specific vision capabilities for reading documents and computer use, and the ability to sit, stand, or walk for prolonged periods.</p><br>

Compounder

<h1><strong>Job Title: Compounder</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a dedicated Compounder to join our team. The successful candidate will comply with all company policies related to employee safety, food safety, quality assurance, and regulatory standards, including Good Manufacturing Practices (GMPs). You will be responsible for setting up and operating assigned mixing machines to ensure finished products meet customer specifications and regulatory requirements. Additionally, you will train and support other employees in the operation of mixing equipment and perform cleaning and sanitization during product changeovers. Your role will involve inspecting machinery before line start-up and after changeovers to ensure readiness, maintaining clear and accurate documentation, and collaborating with coworkers to meet production goals.</p><p><br></p><h2>Responsibilities</h2><ul><li>Set up and operate assigned mixing machines to ensure finished products meet customer specifications and regulatory requirements.</li><li>Use hand tools as needed for machine operations.</li><li>Train and support other employees in the operation of mixing equipment.</li><li>Perform cleaning and sanitization of equipment during product changeovers.</li><li>Inspect machinery before line start-up and after changeovers to ensure readiness.</li><li>Take ownership of mixing outcomes by accurately following work orders and troubleshooting issues.</li><li>Maintain clear, accurate, and legible documentation and records.</li><li>Collaborate with coworkers, including maintenance and quality assurance teams, to meet production goals.</li><li>Provide support to other departments as needed and perform additional duties as assigned.</li><li>Attend all required company training sessions.</li></ul><h2>Essential Skills</h2><ul><li>Production experience, particularly in general production and mixing.</li><li>Understanding and application of Good Manufacturing Practices (GMPs) with at least 2 years of experience.</li><li>Experience in compounding, blending, batching, and batch making.</li><li>Familiarity with FDA regulations.</li><li>Ability to maintain batch records and perform batch mixing.</li><li>Experience in food manufacturing.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Ability to maintain respectful communication with coworkers at all levels within the organization.</li><li>Problem-solving skills for equipment and processes in partnership with maintenance.</li><li>Capability to determine root causes for mistakes/concerns and apply corrective action.</li><li>Ability to read and write English; bilingual in Spanish is preferred.</li><li>Basic math skills.</li><li>Basic computer skills.</li></ul><h2>Work Environment</h2><p>The position offers shifts on both the 1st and 2nd shifts, providing flexibility in work hours. You will be part of a growing company with consistent business, enjoying a family-owned atmosphere with a family feel. The company offers incentives such as gas cards and cookouts. There is also a summer incentive program with additional hourly pay from May 1st to August 30th, and opportunities for merit increases following a 6-month review and annually thereafter.</p>

<h1><strong>Job Title: Pharmacy Technician</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a dedicated Pharmacy Technician to join our team, specializing in compounding and order fulfillment. This role requires meticulous attention to detail and the ability to perform various pharmacy tasks with precision and efficiency.</p><p><br></p><h2>Responsibilities</h2><ul><li>Fulfill orders as the primary function, involving compounding prescriptions through techniques such as weighing, mixing, grinding, levigating, and encapsulating.</li><li>Assist with secondary tasks including answering phones, assisting customers, processing prescriptions, restocking supplies, cleaning, and preparing shipping labels.</li><li>Engage in physical tasks such as lifting containers, standing, walking, bending, and cleaning work areas.</li><li>Use fingers, hands, wrists, forearms, arms, and shoulders continuously in the compounding process and order fulfillment.</li><li>Participate in team meetings and collaborate with lab supervisors and pharmacists on special requests.</li></ul><h2>Essential Skills</h2><ul><li><em>Pharmacy Technician certification or certificate.</em></li><li>CPhT certification.</li><li>Experience with pharmacy software and data entry.</li><li>Strong customer service skills.</li><li><em>1+ year(s) of experience in any pharmacy setting.</em></li><li>Oregon Pharmacy Technician License or Certification required.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High School Diploma/GED.</li><li>Ability to multi-task effectively.</li><li>Strong work ethic with motivation to meet performance metrics.</li><li>Excellent attention to detail and accuracy.</li><li>Time management and prioritization skills.</li><li>Ability to quickly learn new systems and processes.</li><li>Strong communication skills, both verbal and written.</li><li>Reliability and positive attendance record.</li><li>Team player mentality.</li></ul><h2>Work Environment</h2><p>Our facility offers a spacious and comfortable environment with excellent employee areas. The schedule is Monday through Friday, 11:30 AM to 8:00 PM, with every third Saturday required. Benefits include a flexible schedule, health insurance, dental, vision, retirement plans, and a monthly bonus program based on performance. Our pharmacy technicians do not bill insurance, allowing them to focus on compounding and advancing skill sets in various areas. The dress code is professional, aligning with our commitment to excellence.</p>

Compounding Pharmacy Technician

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