<h1><strong>Job Title: Research Coordinator</strong></h1><p><br></p><h2>Job Description</h2><p>Join our dynamic team as a Research Coordinator, where you will play a pivotal role in coordinating clinical trials in compliance with FDA and GCP guidelines. Your contributions will aid in the development of new medications while providing the best participant experience.</p><p><br></p><h2>Responsibilities</h2><ul><li>Coordinate trials per FDA and GCP guidelines.</li><li>Schedule patient visits.</li><li>Input trial data into the Electronic Data Capture system, ensuring quality control for content.</li><li>Collaborate closely with the marketing coordinator for subject recruitment.</li><li>Input visit data into the clinical trial management system (CTMS) to track patient visits and procedures.</li><li>Process required lab specimens, label vials, and accurately fill out requisitions for storage and shipment per study protocols.</li><li>Prepare and maintain research study files.</li><li>Compile, collate, and submit study information within established deadlines.</li></ul><h2>Essential Skills</h2><ul><li>Pre-screening patients</li><li>Clinical research</li><li>Clinical trial</li><li>Patient recruitment</li><li>1 year of clinical research experience</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>BS/BA in life sciences, biology, or educational equivalent, or relevant work experience in a clinical environment or medical setting.</li><li>Ability to establish and maintain effective working relationships with coworkers and clients.</li><li>Basic knowledge of medical terminology.</li><li>Proficient in MS Windows and Office applications such as Access, Outlook, Excel, and Word.</li><li>Ability to quickly learn industry-specific software and experience with social media platforms.</li></ul><h2><br></h2>

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Clinical Research Coordinator

<h1 style="font-weight: 700;">Job Title: Research Coordinator</h1><br><h2>Job Description</h2><p>We are seeking a dedicated Research Coordinator to join our dynamic team in Tulsa, Oklahoma. You will play a crucial role in coordinating clinical trials, ensuring compliance with FDA and GCP guidelines, and contributing to the development of new medications. This position offers an opportunity to be part of a best-in-class clinical research site that is committed to changing lives and providing the community with a wide range of trial opportunities.</p><br><h2>Responsibilities</h2><ul><li>Coordinate clinical trials in accordance with FDA and GCP guidelines.</li><li>Schedule patient visits and manage trial data using the Electronic Data Capture system, ensuring quality control.</li><li>Collaborate with the marketing coordinator to recruit subjects for trials.</li><li>Input visit data into the Clinical Trial Management System (CTMS) to track patient visits and completed procedures.</li><li>Process lab specimens, label vials, and fill out requisitions accurately for storage or shipment as per study protocol.</li><li>Prepare and maintain research study files, compiling and submitting study information within established deadlines.</li></ul><h2>Essential Skills</h2><ul><li>1+ year of clinical research experience.</li><li>Pre-screening patients for clinical trials.</li><li>Expertise in clinical research and patient recruitment.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>BS/BA in life sciences, biology, or equivalent education or relevant work experience in a clinical environment.</li><li>Ability to establish and maintain effective working relationships with coworkers and clients.</li><li>Basic knowledge of medical terminology.</li><li>Proficiency in MS Windows and Office applications like Access, Outlook, Excel, and Word.</li><li>Ability to quickly learn industry-specific software and experience with social media platforms.</li></ul><h2>Work Environment</h2><p>Join our rapidly growing team dedicated to providing the best participant experience during trials. Our work involves trials related to Chohns, Lupus, and Dermatitis, offering a collaborative and supportive environment. Engage with advanced technologies and software to ensure efficient trial management and data processing.</p><br>

<h1><strong>Job Title: Clinical Research Coordinator</strong></h1><h2>Job Description</h2><p>Join our team as a Clinical Research Coordinator and contribute to a groundbreaking study on blinded continuous glucose monitoring. This role involves recruiting and managing participants, collecting and analyzing data, and ensuring the smooth operation of clinical trials.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct chart reviews to identify eligible patients for the study.</li><li>Screen and recruit healthy pregnancies for continuous glucose monitoring.</li><li>Coordinate with various sites to optimize patient scheduling and visits.</li><li>Meet participants at their second prenatal or ultrasound visits to follow procedures and gather consents.</li><li>Collect and enter medical record data accurately.</li><li>Conduct one research visit at the time of randomization to explain study procedures and place glucose monitors.</li><li>Conduct 3-4 patient visits weekly to maintain study integrity.</li></ul><h2>Required Skills &amp; Experience</h2><ul><li>Proficiency in chart review and pre-screening patients.</li><li>Experience in clinical trials, including patient recruitment and consenting.</li><li>Ability to place glucose monitors confidently.</li><li>Bachelor’s degree is required.</li></ul><h2>Work Environment</h2><p>The role involves visiting multiple sites within the Cleveland area. The work schedule will be determined based on patient availability and will be provided in advance.</p>

<p><br></p><p><strong><u>Clinical Research Coordinator</u></strong></p><ul><li>Recruits and consents research participants.</li><li>Conducts telephone or in-person interviews with participants, including screening for</li><li>eligibility.</li><li>Performs follow-up by telephone, e-mail, and/or mail with study participants.</li><li>Prepares, mails, and processes questionnaires and other study correspondence.</li><li>Assists in tracking study participants using MS Excel.</li><li>Keeps accurate and detailed records and files of work.</li><li>Reviews, edits, cleans, and enters participant data into a database.</li><li>May assist with literature reviews for proposal submissions and manuscript preparation.</li><li>Handles bookkeeping related to study budgets, including ordering supplies, requesting checks for payment, and participant incentives.</li><li>Performs miscellaneous administrative tasks such as typing labels, copying, faxing, meeting preparation, note-taking, and transcribing audio files.</li></ul><p><br></p><p><strong><u>Qualifications</u></strong></p><ul><li><strong>MUST have 1+ year of patient facing Clinical Research Coordinator (CRC) experience </strong></li><li>Experience with chart review and patient recruitment</li><li>Knowledge of EDC and EMR systems</li><li>Understanding of clinical research and Good Clinical Practice (GCP)</li><li>Experience in pre-screening patients</li><li>High school diploma or General Education Development (GED) required</li><li>Vaccine experience is a plus</li><li>Phlebotomy experience is a plus</li></ul><h2><br></h2>

<p>Join our dynamic team as a Research Coordinator, where you will play a pivotal role in coordinating clinical trials in compliance with FDA and GCP guidelines. Your contributions will aid in the development of new medications while providing the best participant experience.</p><p><br></p><h2>Responsibilities</h2><ul><li>Coordinate trials per FDA and GCP guidelines.</li><li>Schedule patient visits.</li><li>Input trial data into the Electronic Data Capture system, ensuring quality control for content.</li><li>Collaborate closely with the marketing coordinator for subject recruitment.</li><li>Input visit data into the clinical trial management system (CTMS) to track patient visits and procedures.</li><li>Process required lab specimens, label vials, and accurately fill out requisitions for storage and shipment per study protocols.</li><li>Prepare and maintain research study files.</li><li>Compile, collate, and submit study information within established deadlines.</li></ul><h2>Essential Skills</h2><ul><li>Pre-screening patients</li><li>Clinical research</li><li>Clinical trial</li><li>Patient recruitment</li><li>1 year of clinical research experience</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>BS/BA in life sciences, biology, or educational equivalent, or relevant work experience in a clinical environment or medical setting.</li><li>Ability to establish and maintain effective working relationships with coworkers and clients.</li><li>Basic knowledge of medical terminology.</li><li>Proficient in MS Windows and Office applications such as Access, Outlook, Excel, and Word.</li><li>Ability to quickly learn industry-specific software and experience with social media platforms.</li></ul>

<h1><strong>Job Title: Clinical Research Coordinator - Bristol, TN</strong></h1><p><br></p><h2><strong>Job Description</strong></h2><p>The Research Coordinator will assist an Investigator, Research Associate, or Project Manager with operationalizing the tasks associated with implementing a research study. This position involves a variety of 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, 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></ul><h2><strong>Required Skills &amp; Experience</strong></h2><ul><li>High school diploma or General Education Development (GED).</li><li>6-12 months of clinical research coordinator experience.</li><li>Experience with chart review, patient recruitment, and clinical research.</li><li>Knowledge of EDC, EMR, and GCP.</li><li>Pre-screening patients.</li></ul><h2><strong>Additional Skills &amp; Qualifications</strong></h2><ul><li>Phlebotomy experience is a plus.</li></ul><h2><strong>Work Environment</strong></h2><p>This position requires working onsite for 5 days a week, totaling 40 hours. You will have the opportunity to work in clinical research trials and support one of the leading healthcare providers in the US. The role offers opportunities for advancement, including roles such as CRC II, Team Lead, and Project Manager.</p>

Clinical Research Coordinator (Bristol, TN)

<p>*This is a 40hr/week contract, this position is not currently considering candidates who need to relocate.*</p><p>Previous clinical research experience is required, please read posting carefully before applying.</p><p><br></p><h2><strong>Job Description</strong></h2><p>The Research Coordinator will assist an Investigator, Research Associate, or Project Manager with operationalizing the tasks associated with implementing a research study. This position involves a variety of 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, 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></ul><h2><strong>Required Skills &amp; Experience</strong></h2><ul><li>High school diploma or General Education Development (GED).</li><li>6-12 months of clinical research coordinator experience.</li><li>Experience with chart review, patient recruitment, and clinical research.</li><li>Knowledge of EDC, EMR, and GCP.</li><li>Pre-screening patients.</li></ul><h2><strong>Additional Skills &amp; Qualifications</strong></h2><ul><li>Phlebotomy experience is a plus.</li></ul><h2><strong>Work Environment</strong></h2><p>This position requires working onsite for 5 days a week, totaling 40 hours. You will have the opportunity to work in clinical research trials and support one of the leading healthcare providers in the US. The role offers opportunities for advancement, including roles such as CRC II, Team Lead, and Project Manager</p>

<h1><strong>Job Title: Clinical Research Coordinator</strong></h1><p><br></p><h2><strong>Job Description</strong></h2><p>The Research Coordinator will assist an Investigator, Research Associate, or Project Manager with operationalizing the tasks associated with implementing a research study. This position involves a variety of 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, 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></ul><h2><strong>Required Skills &amp; Experience</strong></h2><ul><li>High school diploma or General Education Development (GED).</li><li>6-12 months of clinical research coordinator experience.</li><li>Experience with chart review, patient recruitment, and clinical research.</li><li>Knowledge of EDC, EMR, and GCP.</li><li>Pre-screening patients.</li></ul><h2><strong>Additional Skills &amp; Qualifications</strong></h2><ul><li>Phlebotomy experience is a plus.</li></ul><h2><strong>Work Environment</strong></h2><p>This position requires working onsite for 5 days a week, totaling 40 hours. You will have the opportunity to work in clinical research trials and support one of the leading healthcare providers in the US. The role offers opportunities for advancement, including roles such as CRC II, Team Lead, and Project Manager.</p>

Clinical Research Coordinator (Knoxville, TN)

<p><strong>Description</strong></p><p>We are actively seeking a driven and adaptable Clinical Research Coordinator to support clinical trials across multiple locations. This is an entry-level role designed for candidates with a hands-on medical <span style="background-color: none; color: rgb(8, 7, 7);"><span style="color: rgb(8, 7, 7); background-color: none;">background</span></span> and strong patient interaction experience, such as medical assistants, phlebotomists, EMTs, or similar roles. As a CRC, you will be part of a growing clinical operations team, gaining direct experience in the coordination of clinical trials. This position offers hands-on learning, mentorship, and full support in developing your clinical research skills.</p><p><br></p><p>Key Responsibilities include (but are not limited to):</p><p>• Assist in executing clinical trial activities under the guidance of experienced team members</p><p>• Support patient-facing responsibilities including scheduling, check-ins, and follow-up communication</p><p>• Participate in subject screening, enrollment, and retention efforts</p><p>• Enter and maintain accurate study data, and assist with resolving queries in electronic data capture (EDC) systems</p><p>• Attend site initiation visits and investigator meetings as needed</p><p>• Prepare and organize study documentation, source materials, and regulatory files</p><p>• Coordinate appointment scheduling and assist in ensuring visit compliance</p><p>• Communicate with site staff, patients, and sponsor or CRO representatives</p><p>• Travel between locations and satellite sites as needed</p><p><br></p><p><strong>Additional Skills &amp; Qualifications</strong></p><p>Required Qualifications:</p><p>• Prior experience as an Ophthalmic Technician or working in ophthalmology is required</p><p>• Strong interpersonal and organizational skills</p><p>• Basic familiarity with medical terminology or healthcare procedures</p><p>• Comfort with technology and ability to learn EDC systems</p><p>• Ability to multitask in a dynamic, detail-oriented environment</p><p>• Willingness to travel to support multiple study sites</p><p>Preferred Qualifications:</p><p>• Fluent in Spanish (spoken and written)</p><p>• Familiarity with clinical trial management systems (CTMS) and electronic regulatoryplatforms</p>

Clinical Research Coordinator (Ophthalmology)

Clinical Research Coordinator - Ames, IA

Clinical Research Coordinator - Lombard, IL

Clinical Research Coordinator - Statesville, NC

Clinical Research Coordinator - Wilmington, NC

<h1><strong>Job Title: Clinical Research Coordinator I</strong></h1><p><br></p><h2>Job Description</h2><p>As a Clinical Research Coordinator I, you will be responsible for coordinating the initiation and activation of all new clinical trial protocols. You will collaborate with Research Nurse Clinicians and physicians to ensure accurate eligibility confirmation and informed consent processes for patients.</p><p><br></p><h2>Responsibilities</h2><ul><li>Coordinate the preparation of study tools such as study binders, medication diaries, eligibility checklists, and flow sheets using Oncore®, Excel®, and Word.</li><li>Review patients&#39; charts and medical history to confirm protocol eligibility and obtain necessary source documents.</li><li>Ensure that IRB approved informed consent forms are obtained, signed, placed in medical records, and copies provided to patients.</li><li>Maintain research records for all patients enrolled in studies, including patient consent, eligibility, Case Report Forms, and registration confirmation.</li><li>Assist in grading adverse events using NCI common toxicity criteria or protocol-specific grading scales.</li><li>Complete Serious/Unexpected Adverse Event forms as required by study sponsors, federal requirements, and institutional guidelines.</li><li>Provide regular reports to tumor study group members and Principal Investigator on assigned studies using Oncore®.</li><li>Serve as a liaison with study sponsors, schedule monitoring visits and conference calls, and respond to sponsors’ queries accurately and timely.</li></ul><h2>Essential Skills</h2><ul><li>2+ years of clinical research experience.</li><li>2+ years of oncology experience.</li><li>Experience in data management, with 60% of the job focused on this area.</li><li>Experience working in multiple EDC systems, with preference for Medidata and Inform.</li><li>Experience recruiting, screening, and consenting patients for clinical trials.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree.</li><li>Experience in gynecology oncology group or similar settings.</li><li>Experience in data collection and data entry.</li></ul><h2>Work Environment</h2><p>The role will be based on-site in the Bronx, requiring presence four times a week. You will work in a dynamic clinical setting, interacting with diverse technologies and systems to support clinical research efforts.</p>

Clinical Research Coordinator I

<h1><strong><em>﻿</em>Clinical Research Coordinator II </strong></h1><p><br></p><h2>Job Description</h2><p>The Clinical Research Coordinator (Non-RN) plays a pivotal role in managing research studies, trials, and programs. This includes patient screening, assessing eligibility, and coordinating the care and follow-up of volunteers participating in research. The coordinator is responsible for recruiting and consenting research participants, providing exceptional patient-facing interactions, and coordinating biospecimen collection through collaboration with clinical research nursing staff, laboratory teams, and hospital departments to ensure compliance with regulations and protocols.</p><p><br></p><h2>Responsibilities</h2><ul><li>Execute and coordinate the informed consent process for participants in clinical trials and research studies across various locations, which may involve travel or the use of technology.</li><li>Oversee all aspects of research, including patient screening, eligibility assessment, and volunteer participation and follow-up.</li><li>Coordinate the recruitment and consenting of research participants for therapeutic areas served.</li><li>Deliver concierge-level service for all patient-facing interactions during clinical trials and research studies.</li><li>Coordinate or perform biospecimen collection (e.g., blood, tissue) and maintain a HIPAA-protected database linking patient information to biospecimens used in research; conduct patient chart review and data collection.</li><li>Collaborate with Clinical Research nursing staff, Research Services, laboratory teams, hospital departments, and physician offices to ensure regulatory and protocol compliance.</li><li>Work with assistant clinical coordinators to ensure compliant data entry/data mining into registries, patient records, and research-specific database systems.</li><li>Assist Principal Investigators and research staff in developing compliant research protocols and control documents.</li><li>Serve as the study-specific point of contact for participants, investigators, research staff, hospital departments, and external research partners.</li><li>Collaborate with clinical research supervisors and staff to implement standard operating procedures (SOP) for the research division, ensuring compliance with clinical research standards and procedures.</li><li>Maintain sensitivity to cost containment measures by conserving hospital supplies, equipment, and human resources while overseeing project budgets from internal and external funding sources.</li></ul><h2>Essential Skills</h2><ul><li>Ability to work independently in a fast-paced clinical or research environment, managing multiple tasks efficiently and timely.</li><li>Knowledge of HIPAA data protection and patient advocacy, or similar ethical treatment awareness in research.</li><li>Effective communication with research participants, investigators, research staff, and external partners.</li><li>Analytical approach to problem solving, fact analysis, and sound judgment application.</li><li>Ability to accept direction and adapt to the evolving needs of clinical research units.</li><li>Proficiency in Microsoft Office applications, including Word, Excel, Access, Outlook, and Internet skills.</li></ul>

Clinical Research Coordinator II

Clinical Research Coordinator II (TRI)

<h1 style="font-weight: 700;">Job Title: Clinical Data Coordinator</h1><br><h2>Job Description</h2><p>Join our dynamic team dedicated to advancing healthcare through meticulous data management and research. As a Clinical Data Coordinator, you will play a crucial role in supporting clinical research efforts by ensuring the accuracy and integrity of data, preparing for audits, and facilitating monitor visits. You will work collaboratively with a specialized team divided by disease group, including a data coordinator, clinical coordinator, regulatory coordinator, and nurse.</p><br><h2>Responsibilities</h2><ul><li>Perform all data entry, data uploads, and address data queries.</li><li>Assist in preparing for audits to ensure compliance.</li><li>Coordinate monitor visits to facilitate research activities.</li><li>Provide additional support work as needed to enhance team efficiency.</li></ul><h2>Essential Skills</h2><ul><li>Proficient in data entry and data management.</li><li>Experience with clinical data, specifically with EMR systems like EPIC.</li><li>Ability to work effectively within a team.</li><li>Adaptable to changing priorities.</li><li>Knowledge in clinical research and oncology.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Oncology experience is a plus.</li><li>Research experience is preferred.</li><li>Certification through SOCRA or ACRP is beneficial for career advancement.</li></ul><h2>Work Environment</h2><p>You will be part of a collaborative team divided by disease group, consisting of a data coordinator, clinical coordinator, regulatory coordinator, and a nurse. The position requires working onsite for three days a week, with the flexibility to work from home for two days. While remote days are flexible, availability for team meetings and monitor visits is essential. Embrace opportunities for growth within the data path or transition into other teams, such as clinical or regulatory, with potential pay increases upon certification.</p><br>

Clinical Research Data Coordinator

<h1><strong>Job Title: Clinical Research Nurse - Oncology Based (Must have onco exp)</strong></h1><p><br></p><h2>Job Description</h2><p>Join a prestigious academic research institute committed to pioneering scientific discoveries in basic, clinical, and population-based cancer research. As a Clinical Research Coordinator, you will play a vital role in reducing cancer incidence, mortality, and morbidity by facilitating high-profile studies and working with state-of-the-art equipment.</p><p><br></p><h2>Responsibilities</h2><ul><li>Screen and enroll subjects into clinical trials.</li><li>Explain the informed consent process to participants.</li><li>Document adverse events during the trial.</li><li>Collect and manage study documents, including protocols, regulatory documents, informed consents, case report forms, and source documents.</li><li>Prepare applications for the Institutional Review Board (IRB).</li></ul><h2>Essential Skills</h2><ul><li>Registered Nurse with a license in the Commonwealth of Pennsylvania.</li><li>Minimum of two to three years of clinical research experience.</li><li>Experience in hematology and cancer medication administration.</li><li>Proficiency in adverse event reporting using CTCAE 4.0.</li><li>Effective communication and writing skills.</li><li>Ability to multi-task and problem solve.</li><li>Demonstrated teamwork and independent working capabilities.</li><li>Knowledge of IRB and human research protection regulations.</li><li>Strong computer skills, particularly in MS Office Suite.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor of Science in Nursing (BSN) preferred.</li><li>Experience in oncology is highly advantageous.</li></ul><h2>Work Environment</h2><p>The role is based in a fast-paced environment on a large campus, offering the opportunity to work with one of the most prestigious academic research institutes globally. You will be involved in high-profile studies with renowned sponsors, utilizing cutting-edge technology.</p>

Clinical Research Nurse

<h1 style="font-weight: 700;">Job Title: Clinical Research Nurse</h1><br><h2>Job Description</h2><p>The Clinical Research Coordinator II RN (CRC-II RN) plays a pivotal role in the research institute, operating under limited supervision to plan, coordinate, evaluate, and perform nursing care for participants, while collecting data for assigned research projects. This role adheres to study-specific protocol guidelines and communicates effectively with Principal Investigators, Sub-Investigators, Clinical Research Leads, and research support staff. The CRC-II RN advocates for patient care while ensuring compliance with industry-sponsored and investigator-initiated clinical trials, following FDA regulations and ICH/GCP guidelines.</p><br><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 the principles of Universal Precautions and abide by HIPAA regulations.</li><li>Maintain a clean and prepared clinical space, performing set-up and turnover procedures according to SOPs.</li><li>Participate in training programs to maintain licensure.</li><li>Utilize positive interpersonal communication skills with healthcare team, patients, investigators, sponsors, and administration.</li><li>Review informed consent documents according to regulations with study candidates or their legal representatives.</li><li>Manage multiple clinical trial protocols, coordinate execution and follow-up, and perform accurate documentation.</li><li>Promote Principal Investigator oversight by advising of deviations in conduct and patient status.</li><li>Coordinate work of support staff, laboratory technicians, and assistants for efficient and high-quality results.</li><li>Serve as liaison between Principal Investigators and the Institutional Review Board and Office of Sponsored Programs.</li><li>Prepare and review documentation for clinical research study startup, execution, modification, renewal, and termination.</li><li>Remain current on regulatory requirements and HIPAA regulations, implementing changes as needed.</li></ul><h2>Essential Skills</h2><ul><li>Clinical research expertise</li><li>Knowledge of Good Clinical Practice (GCP)</li><li>Pre-screening patients</li><li>Registered Nurse qualifications</li><li>IV infusion skills</li><li>Electronic Data Capture (EDC)</li><li>Chart review proficiency</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Associate degree in Nursing</li><li>Minimum 2 years of Clinical Research experience</li><li>Current active State of Florida license as a Registered Nurse</li><li>Basic Life Support (BLS) certification</li></ul><h2>Work Environment</h2><p>This position is based in a hospital setting, requiring adherence to clinical protocols and maintaining professionalism in a dynamic healthcare environment.</p><br>

<p><strong>Description</strong></p><p>The team is 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. </p><ul><li>Perform tasks such as; preparation of investigational products</li><li>Monitoring research subjects</li><li>Taking and recording vital signs</li><li>Performing EKG’s, drawing blood for research and clinical lab samples</li><li>Recording study data in various data bases</li><li>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.</li></ul><p><strong>Qualifications</strong></p><ul><li>New York State licensed RN. </li><li>Bachelor&#39;s degree required. 2-5 years minimum clinical experience. </li><li>Proficient in phlebotomy, basic clinical assessments, IV skills</li><li>Follow a detailed clinical research protocol. </li><li>Excellent organizational skills, problem solving and communication skills required.</li></ul>

<p><strong>Description</strong></p><p>The Upstate Global Health team is 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><ul><li>Perform tasks such as; preparation of investigational products</li><li>Monitoring research subjects</li><li>Taking and recording vital signs</li><li>Performing EKG’s, drawing blood for research and clinical lab samples</li><li>Recording study data in various data bases</li><li>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.</li></ul><p><br></p><p><strong>Additional Skills &amp; Qualifications</strong></p><ul><li>New York State licensed RN. </li><li>Bachelor&#39;s degree required. 2-5 years minimum clinical experience. </li><li>Proficient in phlebotomy, basic clinical assessments, IV skills</li><li>Follow a detailed clinical research protocol. </li><li>Excellent organizational skills, problem solving and communication skills required.</li></ul><p><br></p><p><strong>Experience Level</strong></p><p>Intermediate Level</p>

<p>We are seeking a dedicated and experienced Clinical Research Nurse to join our oncology research team. This role is pivotal in supporting the execution of Phase I–III clinical trials, ensuring compliance with Good Clinical Practice (GCP), and delivering compassionate care to oncology patients participating in research studies.</p><p><br></p><p><strong>Key Responsibilities:</strong></p><ul><li>Coordinate and conduct clinical trial activities including patient screening, enrollment, informed consent, and study visits.</li><li>Administer investigational products and monitor patients for adverse events.</li><li>Collect, document, and manage clinical data in compliance with protocol and regulatory requirements.</li><li>Collaborate with investigators, sponsors, and multidisciplinary teams to ensure protocol adherence and patient safety.</li><li>Prepare for and participate in monitoring visits, audits, and regulatory inspections.</li><li>Educate patients and families about trial participation and procedures.</li></ul><p><strong>Qualifications:</strong></p><ul><li>Registered Nurse (RN) license in good standing.</li><li>Minimum 2 years of clinical research experience, preferably in oncology.</li><li>Familiarity with IRB processes, GCP, and FDA regulations.</li><li>Strong organizational and communication skills.</li><li>Experience with electronic data capture systems and clinical trial documentation.</li></ul><p><br></p>

Clinical Research Nurse (Relocation Offered)

<p style="text-align: center;"><strong>   Clinical Research Nurse Coordinator</strong></p><p><br></p><p>Seeking a Clinical Research Nurse Coordinator with IV infusion experience and strong knowledge of infusion practices. This role supports all phases of clinical trials, includingdrug administration (FDA-approved and investigational), protocol compliance,participant care, data collection, and regulatory reporting.</p><p><br></p><p><strong>Key Responsibilities:</strong></p><ul><li>Partner with Principal Investigator to ensure compliance with FDA, GCP, and sponsor protocols</li><li>Prioritize participant safety and informed consent</li><li>Manage study workflows, documentation, and regulatory submissions</li><li>Screen, recruit, and conduct study visits per protocol</li><li>Report adverse events and protocol deviations</li><li>Handle investigational product logistics and inventory</li><li>Perform clinical assessments and support sponsor audits</li><li>Mentor new staff and contribute to team development</li></ul><p><strong>Qualifications </strong></p><ul><li>RN license with 3+ years of research experience</li><li>IV infusion and phlebotomy experience</li><li>Clinical research and GCP knowledge</li><li>Bachelor’s degree</li><li>EDC and CTMS experience</li><li>CPR, IATA, and GCP certifications</li><li>Specimen handling and patient recruitment skills</li></ul><p><strong>Work Environment:</strong></p><ul><li>Small, collaborative team managing 3–5 studies</li><li>Monday–Friday, 8:00 AM–4:30 PM or 7:00 AM–3:30 PM</li><li>Supportive, growth-oriented culture with open communication</li><li>Mix of high and low volume periods; self-starter mindset valued</li></ul><h1><br></h1>

Clinical Research Nurse Coordinator

<p><strong>LOCATED in Altamonte Springs, FL. Candidates must be open to relocating on their own. </strong></p><p><br></p><p><strong>Clinical Research Nurse Coordinator- Altamonte Springs, FL </strong></p><p>Coordinate and perform nursing care for clinical trial participants under limited supervision</p><p>Ensure compliance with FDA regulations and ICH/GCP guidelines</p><p>Collaborate with Principal Investigators, Sub-Investigators, and research staff</p><p>Serve as a liaison with the IRB and Office of Sponsored Programs</p><p>Support Surgery and Digestive Health research, with a focus on IV infusion and trial execution</p><p><br></p><p><strong><u>Qualifications</u></strong></p><p>Associate degree in Nursing and current RN license</p><p>ACLS certification</p><p>Minimum 2 years of clinical research experience</p><p>Strong IV and infusion skills</p><p>Flexibility to support early OR procedures (approx. once a week)</p><p><br></p><p><br></p>

<h1><strong>Clinical Research Nurse II (Neurology)</strong></h1><p><br></p><h2>Job Description</h2><p>The Clinical Research Nurse II plays a crucial role in planning, coordinating, evaluating, and performing nursing care for participants involved in assigned research projects. Working under limited supervision, this position requires adherence to study-specific protocol guidelines and effective communication with principal investigators, sub-investigators, clinical research leads, and support staff. The role involves advocating for patient care while ensuring compliance with clinical trial protocols, FDA regulations, and ICH/GCP guidelines.</p><p><br></p><h2>Responsibilities</h2><ul><li>Deliver safe care and respect the dignity of all research participants.</li><li>Maintain clinical competencies, including physical assessments, phlebotomy, and IV insertion.</li><li>Adhere to Universal Precautions and HIPAA regulations.</li><li>Ensure the clinical space is clean and prepared, performing set-up and turnover procedures as needed.</li><li>Participate in training programs to maintain licensure.</li><li>Communicate effectively with healthcare team members, patients, investigators, and sponsors.</li><li>Review informed consent documents in accordance with FDA, state, federal, and institutional regulations.</li><li>Manage multiple clinical trial protocols, ensuring accurate and timely documentation.</li><li>Advise the Principal Investigator and other stakeholders of trial deviations and issues affecting trial integrity.</li><li>Coordinate the work of support staff to ensure high-quality results and adherence to protocols.</li></ul><h2>Essential Skills</h2><ul><li>Experience in clinical trials and data collection.</li><li>Proficiency in dose calculations and neurology.</li><li>Ability to perform consenting and data collection tasks.</li><li>Registered Nurse with clinical research experience.</li><li>Understanding of Good Clinical Practice (GCP) guidelines.</li><li>Ability to perform EKG and other study-related tasks.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Ability to perform clinical tasks and assist with minor procedures.</li><li>Adaptability to integrate into various clinical settings.</li><li>Skills in physical assessment, phlebotomy, IV insertion, and investigational drug administration.</li><li>Associate degree in Nursing.</li><li>Minimum of 2 years of clinical research experience.</li><li>Current active State of Florida license as a Registered Nurse.</li><li>Basic Life Support (BLS) certification.</li></ul><h2>Work Environment</h2><p>The role is based in a hospital setting, providing a dynamic and collaborative environment for conducting clinical research.</p>

Clinical Research Nurse II

Clinical Research Nurse II (Neurology)

<p><strong>Clinical Research Patient Recruiters Needed in Richardson, TX!</strong></p><p><strong>Great Opportunity to get a foot into Clinical Research Administration!</strong></p><p>Description:</p><ul><li>Recruit patients for Clinical Research Studies</li><li>Send cold calls and emails</li><li>Follow up with sourced patients</li><li>Other Duties as needed</li></ul><p><strong>Pay: 18.00 USD Hourly</strong></p><p>Schedule: 9:00AM-6:00PM Tuesday-Saturday</p><p>Qualifications:</p><ul><li>Associates or Bachelors in STEM is a plus</li><li>Call Center Experience is a plus</li></ul><h1><br></h1>

Clinical Research Patient Recruiter

<p><strong>Clinical Research Scheduler</strong>  </p><p>&#128205; Richardson, TX | &#128188; Full-Time | &#128176; $18/hr  </p><p><br></p><p><strong>Schedule:</strong> Tuesday–Saturday, 9:00 AM–6:00 PM</p><p><br></p><p>Are you looking to break into clinical research? This is a fantastic opportunity to gain hands-on experience in <strong>patient recruitment and clinical trial support</strong>. If you&#39;re energized by meaningful work, great with people, and thrive in a fast-paced environment—this role could be for you.</p><h3><br></h3><h3><strong>What You’ll Do</strong></h3><ul><li>Make outbound and receive inbound calls, texts, and emails to recruit potential participants for clinical studies</li><li>Conduct phone screenings to assess eligibility based on protocol criteria</li><li>Collaborate with research coordinators to align on recruitment targets and scheduling</li><li>Maintain accurate records and track recruitment progress in databases</li><li>Send appointment reminders, follow-ups, and ensure timely scheduling</li><li>Support ongoing outreach—even between active studies—to keep a strong participant pipeline</li><li>Escalate major findings or trends to leadership as needed</li><li>Attend study-related meetings and contribute to recruitment strategies</li></ul><h3><strong>Qualifications</strong></h3><ul><li>High school diploma required; <strong>Associate’s or Bachelor’s in a STEM field is a plus</strong></li><li>Previous experience in <strong>call center</strong>, patient-facing roles, or healthcare strongly preferred</li><li>Strong communication, organizational, and multitasking skills</li><li>Comfortable with heavy call volume—<strong>up to 100+ calls per day</strong></li><li>Proficient in Microsoft Office; experience with texting platforms or recruitment tools a plus</li><li>Must be a self-starter with a strong work ethic and a &quot;smile-and-dial&quot; attitude</li></ul><p>This is your chance to step into the clinical research world with a supportive team, fast growth potential, and a mission-driven purpose. Apply today to make a difference in the future of medicine!</p>

Clinical Research Scheduler

<h1 style="font-weight: 700;">Job Title: Clinical Rodent Technician</h1><br><h2>Job Description</h2><p>This position involves managing rodent breeding colonies and providing technical support to investigators and veterinarians. The role includes a variety of tasks related to animal care, administrative procedures, and equipment maintenance.</p><br><h2>Responsibilities</h2><ul><li>Manage rodent breeding colonies, including identifying animals through ear tagging and ear notching.</li><li>Set up breeding cages and perform tasks such as weaning animals.</li><li>Collect and submit samples, including tail tips or ear punches for genotyping.</li><li>Record pedigree, births, deaths, and other data electronically.</li><li>Perform cross-foster rederivation.</li><li>Maintain detailed records on Excel, Word, and other platforms for billing purposes.</li><li>Provide weekly colony reports to investigators and veterinarians.</li><li>Order animals and supplies and maintain equipment.</li><li>Coordinate with husbandry personnel to ensure animal care.</li><li>Assist in training researchers and maintaining equipment like isoflurane gas machines.</li><li>Follow safety protocols and help implement SOPs, guidelines, and related documents.</li><li>Maintain strict infection control procedures.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in animal handling and research.</li><li>Knowledge of husbandry and animal husbandry practices.</li><li>Experience in veterinary tech and rodent handling.</li><li>Understanding of animal science, biology, and health.</li><li>Skills in cleaning, sterilization, and laboratory procedures.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree is preferred but experience may be considered in lieu of education.</li></ul><h2>Work Environment</h2><p>The position is based in an animal research lab, offering extensive experience with high-volume animal care. The lab is part of a top-funded research university, providing a professional and collaborative environment.</p><br>

Clinical Rodent Technician

<h1 style="font-weight: 700;">Job Title: Clinical Supply Chain Manager</h1><br><h2>Job Description</h2><p>The Clinical Supply Chain Manager will ensure the effective management of drug manufacturing and the clinical supply chain, ensuring seamless provision of drug and ancillary supplies across the clinical portfolio. This role requires collaboration with internal clinical supply chain, clinical operation, regulatory, and manufacturing colleagues to assist in the delivery of clinical supplies in line with regulatory requirements and internal quality processes.</p><br><h2>Responsibilities</h2><ul><li>Lead and provide direction around Supply Chain discussions in team meetings, maintaining effective communication with customers and partners.</li><li>Set up the clinical supply chain strategy for studies and/or clinical portfolio of studies.</li><li>Design and implement labeling, packaging, and supply strategies that meet study design, clinical study sites, and regulatory authority requirements, while maximizing supply efficiency.</li><li>Manage, with input from CMC and Regulatory groups, the generation and approval of label texts, translations (where required), and label proof.</li><li>Produce a clinical supply agreement document detailing the design, setup, and operation of the supply chain for responsible studies or groups of studies.</li></ul><h2>Essential Skills</h2><ul><li>Experience in supply chain management and clinical supplies.</li><li>Knowledge of IRT, Cold Chain, GxP, GmP, and regulatory compliance.</li><li>Vendor management and pharmaceutical forecasting expertise.</li><li>Proficiency in budget management, labeling, and shipping processes.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Degree or higher in a relevant scientific subject or business management, or equivalent industry experience.</li><li>Masters or PhD in a relevant scientific subject is desirable.</li><li>Demonstrated computer skills with a functional knowledge of Microsoft packages (MS Word, Excel, Power Point, Outlook, MS Project, SharePoint).</li></ul><h2>Work Environment</h2><p>This role requires a presence on-site three to four days a week, either in Conshohocken, PA or Gaithersburg, MD. Join a leading T-Cell Oncology biotech company with a strong pipeline and an approved product on the market, offering opportunities for long-term growth into <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">senior</span></span> positions.</p><br>

Clinical Supply Chain Manager

<h1><strong>Job Title: Clinical Trials Administrative Support Specialist</strong></h1><p><br></p><h2>Job Description</h2><p>Join a professional, customer-focused pharmaceutical company as a Clinical Trials Administrative Support Specialist. This role involves supporting the maintenance of study records and coordinating study activities. You will develop, maintain, and archive files and records related to multiple clinical trials while providing administrative support. This position offers a competitive salary and a full benefits package.</p><p><br></p><h2>Responsibilities</h2><ul><li>Work with the Project Management team to assist in planning investigator meetings.</li><li>Develop required materials, including training tools.</li><li>Initiate contract/budget requests, track status, and negotiate budgets with sites and vendors if necessary.</li><li>Participate in vendor selection and management.</li><li>Identify changes in the scope of work.</li><li>Formulate, track, measure, and maintain a project-specific matrix and timelines.</li><li>Schedule and manage agenda updates and meeting minutes for project team meetings.</li><li>Develop monthly reports, newsletters, and communication trackers.</li><li>Provide administrative support such as mass site communication distribution, shipping, filing, tracking, and summarization.</li><li>Assist in the clinical trial insurance process by tracking approvals, revisions, and renewals of certificates.</li><li>Maintain and track all project-specific invoices.</li><li>Ensure a smooth site start-up process prior to Site Initiation Visits.</li><li>Assist the Clinical Operations team with maintaining the trial master file, study site records, and files.</li><li>Review essential study documents.</li><li>Develop project-specific procedural documents as needed.</li><li>Prepare and ship IRB/EC dossiers.</li><li>Assist the study team with training and access management for CTMS and other trial-related applications.</li><li>Prepare for study-specific audits and inspections.</li><li>Perform other duties as assigned by <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">senior</span></span> management.</li></ul><h2>Essential Skills</h2><ul><li>Proficient in Microsoft Office (Word, Excel, PowerPoint).</li><li>Well-organized with strong attention to detail.</li><li>Excellent verbal and written communication skills.</li><li>Fluent in English; other languages are a plus.</li><li>Ability to work independently and with flexibility to accommodate international meeting schedules.</li><li>Strong interpersonal skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Minimum of an associate’s degree; bachelor’s degree preferred.</li><li>Previous experience in a healthcare company.</li><li>Experience with trial master file maintenance, auditing, and reconciliation preferred.</li><li>Experience with archival of paper files and auditing archived files.</li><li>Meeting agenda and minute-taking experience.</li><li>Experience interacting with Contract Research Organizations and third-party vendors.</li><li>Experience with Electronic Trial Master File systems.</li><li>Experience in clinical trial management systems.</li></ul>

Clinical Trial Associate

<h2><strong>Job Description</strong></h2><p>We are seeking a dedicated Clinical Research Coordinator to join our dynamic research team. The successful candidate will manage multiple research trials, including first-in-human through phase 3 trials, ensuring compliance with FDA guidelines and adherence to Good Clinical Practice (GCP). This role involves daily interactions with clinicians, sponsors, IRB, regulatory agencies, and other research professionals. As a subject/patient-facing position, strong communication skills are essential for collecting detailed clinical information and sharing it with the study team. The coordinator will be responsible for all aspects of trial conduct, including IRB submission, regulatory documentation, staff training, and overseeing subject enrollment.</p><p><br></p><h2><strong>Responsibilities</strong></h2><ul><li>Accurately prepare and maintain regulatory documents.</li><li>Prepare Informed Consent Documents with institutional language.</li><li>Interface with the IRB, preparing all required documents and submitting packages for review.</li><li>Collaborate with the recruitment team to create advertising plans and enroll subjects.</li><li>Monitor each subject’s schedule for compliance with the protocol.</li><li>Attend study meetings both internally and externally.</li><li>Train the study team on new and amended protocols.</li><li>Assist in operational planning for study visits, communicating needs to administration.</li><li>Create source documents to collect required data in RedCap and oversee team entries.</li><li>Assist in the execution of Informed Consent.</li><li>Enter data into study-specific databases.</li><li>Oversee the ordering, receipt, and maintenance of study supplies.</li><li>Communicate regular study updates with administration.</li><li>Oversee clinic activities as assigned.</li><li>Perform clinical activities as experience and delegation allow.</li><li>Perform on-call duties during evenings and weekends as assigned.</li></ul><h2><strong>Essential Skills</strong></h2><ul><li>Clinical research coordination, screening, enrolling, and regulatory knowledge.</li><li>Proficiency in Microsoft Office products, including Excel.</li><li>Experience with clinical documentation and HIPAA guidelines.</li><li>RedCap and various clinical databases proficiency.</li><li>5+ years of clinical research experience</li></ul><h2><strong>Additional Skills &amp; Qualifications</strong></h2><ul><li>Associates or Bachelor’s degree in a clinical or scientific field, or clinical certificate/license</li><li>Cardiology experience preferred</li><li>Clinical skills, including phlebotomy, ability to take and record accurate vital signs, obtain EKG tracings, and familiarity with medical terminology preferred.</li><li>Clinical Research certification by SoCRA or ACRP.</li></ul><h2><strong>Work Environment</strong></h2><p>This position operates in an office environment, interacting with clinical research patients for screening, consenting, and enrolling in clinical trials. The role requires flexible availability and may involve on-call duties during evenings and weekends.</p>

Clinical Trial Specialist

<h1><strong>IMMEDIATE: CMM Programmer</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking an experienced CMM Programmer with expertise in using PC-DMIS software. The ideal candidate will have a comprehensive understanding of GD&amp;T, be adept at programming complex parts, and possess machining experience to thrive in a machine shop environment.</p><p><br></p><h2>Responsibilities</h2><ul><li>Interpret engineering drawings, specifications, and GD&amp;T requirements to create effective and efficient CMM programs.</li><li>Develop, modify, and optimize CMM programs using PC-DMIS software.</li><li>Design and develop CMM fixturing and tooling to streamline setups.</li><li>Execute CMM programs and analyze results to ensure compliance with quality standards.</li><li>Conduct first-article and in-process inspections.</li><li>Mark parts effectively with machining moves to meet customer specifications.</li><li>Collaborate with engineering and production teams to troubleshoot measurement issues and implement corrective actions.</li><li>Train and mentor staff on CMM programming and measurement techniques as needed.</li><li>Participate in continuous improvement initiatives to enhance measurement processes and efficiency.</li><li>Complete 100% dimensional layouts for PPAP as required.</li><li>Operate multiple CMMs simultaneously to support production checks during the shift.</li><li>Perform routine maintenance and calibration of CMM equipment to ensure accuracy and reliability.</li><li>Stay updated with advances in CMM technologies and measurement techniques.</li></ul><h2>Essential Skills</h2><ul><li>Degree in Manufacturing Engineering, Quality Assurance, or a related field, or equivalent work experience.</li><li>Proven experience as a CMM programmer using PC-DMIS software for complex parts.</li><li>Strong understanding of geometric dimensioning and tolerancing (GD&amp;T) principles.</li><li>Familiarity with CAD software and the ability to read technical drawings.</li><li>Excellent analytical and problem-solving skills.</li><li>Attention to detail and commitment to quality standards.</li><li>Effective communication skills and ability to work collaboratively in a team setting.</li><li>Knowledge of statistical process control (SPC) methodologies.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Certification in metrology or quality control (ASQ, Six Sigma, etc.) is a plus.</li><li>Experience with different types of measuring equipment, such as laser scanners and optical comparators, is desirable.</li><li>Knowledge of casting and machining is preferred.</li></ul><h2>Work Environment</h2><p>The work environment includes a quality lab equipped with four CMMs, where 90% of the workday will be spent. The lab is air-conditioned and clean, while the shop floor is a CNC machine shop with multiple buildings inside the main building. The plant is air-conditioned and well-lit, except for the shipping dock. The position involves working five days a week with flexible hours, including options such as 5am-1:30pm, 6am-2:30pm, or 7am-3:30pm. No overtime is required, and an unpaid lunch break is included. A CMM Operator will assist in this role. </p>

Cmm Programmer

<h1><strong>Job Title: CMM Programmer</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking an experienced CMM Programmer with expertise in using PC-DMIS software. The ideal candidate will have a comprehensive understanding of GD&amp;T, be adept at programming complex parts, and possess machining experience to thrive in a machine shop environment.</p><p><br></p><h2>Responsibilities</h2><ul><li>Interpret engineering drawings, specifications, and GD&amp;T requirements to create effective and efficient CMM programs.</li><li>Develop, modify, and optimize CMM programs using PC-DMIS software.</li><li>Design and develop CMM fixturing and tooling to streamline setups.</li><li>Execute CMM programs and analyze results to ensure compliance with quality standards.</li><li>Conduct first-article and in-process inspections.</li><li>Mark parts effectively with machining moves to meet customer specifications.</li><li>Collaborate with engineering and production teams to troubleshoot measurement issues and implement corrective actions.</li><li>Train and mentor staff on CMM programming and measurement techniques as needed.</li><li>Participate in continuous improvement initiatives to enhance measurement processes and efficiency.</li><li>Complete 100% dimensional layouts for PPAP as required.</li><li>Operate multiple CMMs simultaneously to support production checks during the shift.</li><li>Perform routine maintenance and calibration of CMM equipment to ensure accuracy and reliability.</li><li>Stay updated with advances in CMM technologies and measurement techniques.</li></ul><h2>Essential Skills</h2><ul><li>Degree in Manufacturing Engineering, Quality Assurance, or a related field, or equivalent work experience.</li><li>Proven experience as a CMM programmer using PC-DMIS software for complex parts.</li><li>Strong understanding of geometric dimensioning and tolerancing (GD&amp;T) principles.</li><li>Familiarity with CAD software and the ability to read technical drawings.</li><li>Excellent analytical and problem-solving skills.</li><li>Attention to detail and commitment to quality standards.</li><li>Effective communication skills and ability to work collaboratively in a team setting.</li><li>Knowledge of statistical process control (SPC) methodologies.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Certification in metrology or quality control (ASQ, Six Sigma, etc.) is a plus.</li><li>Experience with different types of measuring equipment, such as laser scanners and optical comparators, is desirable.</li><li>Knowledge of casting and machining is preferred.</li></ul><h2>Work Environment</h2><p>The work environment includes a quality lab equipped with four CMMs, where 90% of the workday will be spent. The lab is air-conditioned and clean, while the shop floor is a CNC machine shop with multiple buildings inside the main building. The plant is air-conditioned and well-lit, except for the shipping dock. The position involves working five days a week with flexible hours, including options such as 5am-1:30pm, 6am-2:30pm, or 7am-3:30pm. No overtime is required, and an unpaid lunch break is included. A CMM Operator will assist in this role. The company operates two shifts: 5am-3:30pm and 3:30pm-2am.</p>

<h1 style="font-weight: 700;">Job Title: CNC Programmer and Machinist</h1><br><h2>Job Description</h2><p>We are seeking an experienced CNC Programmer with expertise in MazaCAM programming for QT-450M machines. This short-term contract position requires travel to Italy one week per month, offering an exciting opportunity to apply your strong programming skills, hands-on machining experience, and process optimization abilities for efficiency and precision.</p><br><h2>Responsibilities</h2><ul><li>Program and operate CNC machines with MazaCAM for QT-450M.</li><li>Set up, troubleshoot, and optimize CNC lathe processes.</li><li>Read and interpret blueprints, GD&amp;T, and technical drawings.</li><li>Ensure machining precision and efficiency.</li><li>Collaborate within a team environment while working independently.</li><li>Travel to Italy one week per month for on-site operations.</li></ul><h2>Essential Skills</h2><ul><li>Proven experience in CNC programming with MazaCAM.</li><li>Strong knowledge of GD&amp;T, tooling, and machining best practices.</li><li>Ability to read and interpret technical drawings.</li><li>Experience in CNC lathe setup and troubleshooting.</li><li>Strong problem-solving skills.</li><li>Attention to detail.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Ability to work independently and in a team environment.</li><li>Willingness to travel to Italy one week per month.</li></ul><h2>Work Environment</h2><p>This is an onsite role with eligibility to travel and work out of our Padua, Italy location if interested. The position offers a flexible schedule as long as it is within the first shift.</p><br>

Cnc Machinist And Programmer

<h1><strong>Job Title: CNC Programmer</strong></h1><p><br></p><h2>Job Description</h2><p>Utilize integration software such as Esprit to transfer engineered models from SolidWorks into machine language on an offline workstation. This allows CNC programs to be simulated before downloading to improve quality, machinability, and equipment throughput. Create a centralized location on the company network to store proven programs for download to various CNC machines. Collaborate with department tech leads to refine programs and seek opportunities to reduce cycle times on the shop floor. Evaluate and analyze new and revised engineering drawings/models for accuracy, manufacturability, and feasibility. Initiate, evaluate, and implement process improvements focused on cost reductions, quality improvements, and safety. Interface with other departments to resolve issues and enhance manufacturability while creating or revising machining processes.</p><p><br></p><h2>Responsibilities</h2><ul><li>Transfer engineered models into machine language using appropriate integration software.</li><li>Simulate CNC programs prior to download to enhance quality and throughput.</li><li>Establish a centralized program repository on the company network.</li><li>Collaborate with tech leads to refine CNC programs and reduce cycle times.</li><li>Evaluate engineering drawings and models for accuracy and manufacturability.</li><li>Initiate and implement process improvements for cost reduction and quality enhancement.</li><li>Work with other departments to resolve machining process issues and improve manufacturability.</li></ul><h2>Essential Skills</h2><ul><li>Minimum 5 years of CNC Programming experience, specifically with lathes.</li><li>Proficiency in programming twin spindle and multi turret lathes.</li><li>Experience with programming Index, Citizen, and Okuma lathes.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Proficiency in CNC lathe and CNC programming.</li><li>Experience with Esprit and Swiss lathe programming.</li></ul><h2>Work Environment</h2><p>This facility uses advanced technologies and requires collaboration with various departments to enhance manufacturing processes.</p>

Cnc Programmer

<h1 style="font-weight: 700;">Job Title: Programmer</h1><br><h2>Job Description</h2><p>This role primarily involves working on CAD/CAM software and designing tooling used to assemble parts, ensuring a seamless handoff to production. The position encompasses setting up machines, running mills and lathes, and engaging in fabrication and functional testing.</p><br><h2>Responsibilities</h2><ul><li>Set up and operate machine tools such as manual and CNC mills and lathes or grinders to machine parts to specifications without supervision.</li><li>Verify conformance of parts to specifications using measuring instruments.</li><li>Analyze written specifications, drawings, rough sketches, shop drawings, and verbal instructions to plan layout and determine the sequence of operations for machining processes.</li><li>Engage in 3D modeling and CAM experience.</li><li>Build fixtures and tooling for prototype parts and equipment.</li><li>Select metal stock and lay out designs according to dimensions computed from scale drawings.</li><li>Understand and interpret multi-view drawings.</li><li>Report immediately all suspicious and hazardous conditions to a supervisor.</li><li>Observe and adhere to all safety guidelines, ensuring quality and safety by complying with all appropriate policies and procedures.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in programming and tool and die making.</li><li>Experience with Mastercam, lathe, and mill operations.</li><li>Solidworks and CNC programming skills.</li><li>CMM programming and CAM experience.</li><li>Prototype fabrication and machine setup.</li><li>Tooling design expertise.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Possess a positive attitude and willingness to work in a team environment.</li><li>Ability to collaborate effectively with others.</li></ul><h2>Work Environment</h2><p>Located in Carson City, the work environment features a campus with various buildings and an airport, emphasizing a family-oriented atmosphere. The position entails a standard 40-hour work week with flexibility, allowing you to create a schedule that fits your needs, typically from 7:00 AM to 3:30 PM. The company promotes respectful communication, positive attitudes, active listening, and timely task execution with minimal errors. Benefits include comprehensive medical, vision, dental, life insurance, disability coverage, a 401(k) plan with company matching, paid vacation, sick days, holidays, tuition assistance, and fitness reimbursement.</p><br>

<h1>Actalent is looking to add a CNC Programmer to our client&#39;s team, a national leader in air compressors!</h1><p><br></p><h2>Job Description</h2><p>Utilize integration software such as Esprit to transfer engineered models from SolidWorks into machine language on an offline workstation. This allows CNC programs to be simulated before downloading to improve quality, machinability, and equipment throughput. Create a centralized location on the company network to store proven programs for download to various CNC machines. Collaborate with department tech leads to refine programs and seek opportunities to reduce cycle times on the shop floor. Evaluate and analyze new and revised engineering drawings/models for accuracy, manufacturability, and feasibility. Initiate, evaluate, and implement process improvements focused on cost reductions, quality improvements, and safety. Interface with other departments to resolve issues and enhance manufacturability while creating or revising machining processes.</p><p><br></p><h2>Responsibilities</h2><ul><li>Transfer engineered models into machine language using appropriate integration software.</li><li>Simulate CNC programs prior to download to enhance quality and throughput.</li><li>Establish a centralized program repository on the company network.</li><li>Collaborate with tech leads to refine CNC programs and reduce cycle times.</li><li>Evaluate engineering drawings and models for accuracy and manufacturability.</li><li>Initiate and implement process improvements for cost reduction and quality enhancement.</li><li>Work with other departments to resolve machining process issues and improve manufacturability.</li></ul><h2>Essential Skills</h2><ul><li>Minimum 5 years of CNC Programming experience, specifically with lathes.</li><li>Proficiency in programming twin spindle and multi turret lathes.</li><li>Experience with programming Index, Citizen, and Okuma lathes.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Proficiency in CNC lathe and CNC programming.</li><li>Experience with Esprit and Swiss lathe programming.</li></ul><h2>Work Environment</h2><p>This facility uses advanced technologies and requires collaboration with various departments to enhance manufacturing processes.</p>

<h1 style="font-weight: 700;">Job Title: CNC Programmer</h1><br><h2>Job Description</h2><p>The CNC Programmer is responsible for creating computer numerically controlled (CNC) programs to automate machinists’ tools using computer-generated electronic data.</p><br><h2>Responsibilities</h2><ul><li>Develop CNC programs to automate machining processes.</li><li>Utilize CAD/CAM software, with a preference for NX, to create and optimize tool paths.</li><li>Analyze blueprints and geometric dimensioning and tolerancing (GD&amp;T) to ensure precision in machining.</li><li>Collaborate with the aerospace engineering team to ensure compliance with industry standards and specifications.</li><li>Select and design appropriate tooling and determine optimal speeds and feeds based on materials and processes.</li><li>Manage outsourced manufacturing processes including plating, surface treatments, and heat treatments.</li><li>Communicate effectively in both written and verbal formats to facilitate project completion.</li><li>Maintain strong attention to detail and manage time effectively to meet multiple deadlines.</li><li>Provide excellent interpersonal and customer service skills, maintaining a positive attitude under pressure.</li></ul><h2>Essential Skills</h2><ul><li>Proven experience in CNC programming.</li><li>Proficiency in CAD/CAM software, particularly NX.</li><li>Analytical skills to gather, process, and interpret data.</li><li>Advanced knowledge in the Aerospace Manufacturing industry, including standards and specifications.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience as a Processing Engineer is preferred.</li><li>Proficiency in Microsoft Office applications.</li><li>Ability to work independently and complete assignments within given parameters.</li><li>Strong organizational and time management skills.</li><li>Ability to provide exemplary customer service under pressure.</li></ul><h2>Work Environment</h2><p>The work environment includes normal production settings with exposure to high noise levels from operating machines, physical hazards from moving equipment and sharp machine parts, and potential exposure to fumes, dust, and mist. Employees may experience skin exposure to oil and cutting fluid, sharp metal edges, and forklifts. The role may require travel between Southwick and Westfield facilities.</p><br>

<h1><strong>Job Title: Sheet Metal Machine Programmer</strong></h1><p><br></p><h2>Job Description</h2><p>We are looking for an experienced Sheet Metal Machine Programmer to join our fabrication team. You will be working for a leader in industrial automation and control systems, committed to delivering innovative solutions and exceptional service to clients globally across various industries. </p><p><br></p><p>This role focuses on creating accurate CNC programs for laser cutting, punching, tube laser, and bending machines using Trumpf TruTops Boost. Candidates should be skilled in reading engineering drawings, selecting proper tooling, and determining optimal bend sequences. A strong understanding of sheet metal fabrication processes and material optimization is essential. The ideal candidate will have hands-on experience with MRP/ERP systems and a sharp eye for detail. You&#39;ll work closely with engineers and operators to troubleshoot issues, improve workflow, and support production efficiency in a fast-paced 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 going to punch, lasers, and press brakes.</li><li>Develop CNC programs for laser cutting, punching, tube laser, and bending machines utilizing Trumpf TruTops Boost.</li><li>Select proper 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>Brainstorm and collaborate with team members to optimize productivity.</li><li>Troubleshoot issues related to CAD/CAM outputs, nesting errors, and machine compatibility.</li><li>Complete work in an accurate and timely manner with attention to detail.</li></ul><h2>Essential Skills</h2><ul><li>5+ years experience in sheet metal fabrication.</li><li>3+ years of experience with Trumpf TruTops Boost software.</li><li>Familiarity with MRP/ERP software for fabrication workflows.</li><li>Strong work ethic and high attention to detail.</li><li>Demonstrated ability to read blueprints and develop optimal tool paths and setups with high accuracy and 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>Work Environment</h2><p>The position is primarily an office environment with factory floor time for collaboration meetings. Expected working hours are 40 per week, with scheduling options including 4x10, 5x8, 8-hour shifts, and day shifts.</p>

<h3><strong>Job Title: Sheet Metal Machine Programmer</strong></h3><p><strong>Location: On-site | Flexible shifts available (4x10, 5x8, or standard day shifts)</strong></p><p><strong>Industry: Industrial Automation &amp; Control Systems</strong></p><p><strong>Type: Full-Time | Direct Hire | Full Benefits</strong></p><hr><h3><strong>About the Role</strong></h3><p>Are you passionate about precision, problem-solving, and cutting-edge fabrication technology? Join a global leader in industrial automation as a Sheet Metal Machine Programmer, where your expertise will directly shape the future of smart manufacturing.</p><p>In this role, you’ll be the brains behind the machines—programming advanced CNC equipment for laser cutting, punching, tube laser, and bending operations. You’ll work with Trumpf TruTops Boost to turn engineering drawings into high-performance parts, collaborating closely with engineers and operators to streamline production and drive innovation.</p><hr><h3><strong>What You’ll Do</strong></h3><ul><li>Program CNC machines using Trumpf TruTops Boost to support laser cutting, punching, tube laser, and press brake operations.</li><li>Calculate bend deductions and generate flat patterns to ensure precision and efficiency.</li><li>Select the right tooling and determine optimal bend sequences based on material type and thickness.</li><li>Interpret engineering drawings and work orders to create accurate, production-ready programs.</li><li>Collaborate with engineers and shop floor teams to troubleshoot issues and improve workflow.</li><li>Optimize material usage and machine compatibility through smart nesting and tool path strategies.</li><li>Maintain high standards of accuracy, quality, and timeliness in a fast-paced environment.</li></ul><hr><h3><strong>What You Bring</strong></h3><ul><li>5+ years of hands-on experience in sheet metal fabrication.</li><li>3+ years of experience programming with Trumpf TruTops Boost.</li><li>Strong understanding of MRP/ERP systems and how they support fabrication workflows.</li><li>Proven ability to read blueprints and develop efficient tool paths with minimal waste.</li><li>Excellent communication skills and a collaborative mindset.</li><li>High attention to detail and a strong work ethic.</li><li>Ability to multitask and adapt in a dynamic, team-oriented manufacturing environment.</li><li>Solid problem-solving skills and a proactive approach to continuous improvement.</li></ul><hr><h3>Work Environment</h3><h1>This role is primarily office-based with regular collaboration on the factory floor. You’ll be part of a forward-thinking team that values innovation, precision, and teamwork—working together to deliver world-class solutions to clients across industries.</h1>

<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 Esprit and/or 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 Esprit and/or 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 lathe and CNC mill operations.</li><li>Expertise in Mastercam and Esprit software.</li><li>Knowledge of GD&amp;T and CNC programming.</li><li>Minimum of 10 years of experience in programming multi-axis CNC lathes 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: Mechanical Process Engineer - Combustion</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a skilled Combustion Engineer to optimize process equipment for improving quality and capacity in thermal processes. You will play a critical role in solving equipment and process problems, driving resolutions for chronic issues, and developing standard practices for thermal and combustion safety processes. Your expertise will be crucial in identifying improvement opportunities and facilitating technology transfer.</p><p><br></p><h2>Responsibilities</h2><ul><li>Optimize process equipment to improve quality and capacity.</li><li>Solve equipment and process problems for thermal processes.</li><li>Lead problem-solving teams and organize support from other resources when necessary.</li><li>Develop and deploy standard practices for thermal and combustion safety processes.</li><li>Maintain working relationships with vendors of thermal and combustion equipment.</li><li>Provide engineering and operational support for large capital improvement projects.</li><li>Sponsor, participate, and occasionally lead development projects.</li><li>Advise plant resources on capital and process solutions.</li><li>Participate in technical assessments of facilities and individual pieces of equipment.</li><li>Provide equipment, control, and process training to the technical base.</li><li>Navigate Rockwell PLCs for troubleshooting.</li></ul><h2>Essential Skills</h2><ul><li>Experience working on and troubleshooting large industrial furnaces.</li><li>Engineering Degree.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in Electrical or Mechanical Engineering or related field from an accredited institution.</li><li>5 years of manufacturing experience.</li><li>3 years in Thermal and Combustion Safety.</li></ul><h2>Work Environment</h2><p>This role is based in an on-site manufacturing environment with standard hours from Monday to Friday, 8 AM to 5 PM. The position involves extensive travel, approximately 50%, including international trips. Employees must be legally authorized to work in the United States, and verification of employment eligibility will be required at the time of hire. Visa sponsorship is not available for this position. Additionally, this position requires access to controlled technology as defined in the Export Administration Regulations and/or the International Traffic in Arms Regulations, where authorizations from the relevant government agency may be necessary to meet export control compliance requirements</p>

Combustion Engineer

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