Clinical Research Coordinator

Job Description

Job Description

Job Title: Clinical Research Coordinator

• Coordinate and manage all aspects of assigned Phase 2–4 clinical trials from site initiation to close-out.
• Conduct study visits, including obtaining informed consent and performing protocol-required procedures.
• Collect source data using eSource systems and ensure timely and accurate entry into eCRFs.
• Utilize eSource, eConsent, eISF, and other clinical trial software platforms to maintain study records.
• Support site readiness and compliance with 21 CFR Part 11, ICH GCP, and sponsor SOPs.
• Maintain up-to-date regulatory documents and study binders.
• Assist with preparation for sponsor, CRO, or regulatory audits.
• Recruit, screen, and enroll study participants according to protocol inclusion/exclusion criteria.
• Ensure ongoing patient safety by monitoring for adverse events and reporting per protocol.
• Serve as the primary point of contact for sponsors, CROs, monitors, and other site staff.
• Support training and mentoring of new CRC staff as assigned.
• Provide on-site support at additional study locations when required, with occasional travel for audits, site visits, or team meetings.

Essential Skills

• MUST HAVE 1 YEAR OF patient facing Clinical Research Coordinator experience
• MUST HAVE Phlebotomy experience
• Good Clinical Practice (GCP)
• Phlebotomy experience
• Experience with eSource, eConsent, and eISF
• Familiarity with 21 CFR Part 11 and ICH GCP

Pay and Benefits

The pay range for this position is $30.00 - $35.00/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 Detroit,MI.

Application Deadline

This position is anticipated to close on Oct 22, 2025.

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 [email protected] for other accommodation options.