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Clinical Research Coordinator

Actalent

Posted Tuesday, December 9, 2025

Posting ID: JP-005713889

Tyler, TX
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Job Title: Clinical Research Coordinator - 6 month contract to hire

Job Description

We are seeking a dedicated and experienced Clinical Research Coordinator to oversee the study coordination, including study start-up, patient recruitment, and providing backup support at our site. This role is pivotal in ensuring the smooth operation of clinical trials, aligning with the highest standards of clinical research.

Responsibilities

  • Serve as the primary contact to ensure appropriate communications, trial management, and adherence to timelines.
  • Coordinate the operational aspects of new and ongoing clinical trials at the site.
  • Work under the supervision of the Principal Investigator(s), exercising excellent clinical judgment in patient monitoring and care.
  • Maintain daily contact with the Principal Investigator(s) for recruitment activities, study start-up, and general communication.
  • Execute the protocol and ensure that all staff working on any given protocol are properly delegated by the Principal Investigator and adequately trained.
  • Recruit and pre-screen patients for the study.
  • Maintain and submit IRB communications and regulatory documents.
  • Communicate in a timely manner with internal teams, investigators, review boards, and study subjects.
  • Prepare study materials as requested by the Principal Investigator, such as informed consent documents, case report forms, enrollment logs, and drug/device accountability logs.
  • Perform other duties as assigned.

Required Skills & Qualifications

  • Minimum of 2 years of experience as a Clinical Research Coordinator.
  • Good management and organizational skills, with a strong understanding of medical procedures.
  • Exceptional interpersonal skills and the ability to work independently.
Job Type & Location

This is a Contract position based out of Tyler, TX.

Pay and Benefits

The pay range for this position is $30.00 - $40.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Tyler,TX.

Application Deadline

This position is anticipated to close on Dec 16, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Compensation:$30-$40

Contact Information

Email: mscherlacher@actalentservices.com

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
On-Site
Communication
Coordinating
Management
Accountability
Clinical Research
Clinical Trials
Innovation
Organizational Skills
Interpersonal Communications
Informed Consent
Case Report Forms
Critical Illness Insurance
Visionary
Institutional Review Board (IRB)
Clinical Research Coordination
Patient Monitoring

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