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Freelance Clinical Research Assistant information

See Rochester, MI salary details

$10

$18

$26

How much do freelance clinical research assistant jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for freelance clinical research assistant in Rochester, MI is $18.62, according to ZipRecruiter salary data. Most workers in this role earn between $15.29 and $21.44 per hour, depending on experience, location, and employer.

What does a freelance clinical research assistant do?

A Freelance Clinical Research Assistant supports clinical trials and research studies on a contract or project basis, rather than as a full-time employee. Their responsibilities typically include data collection, monitoring study participants, ensuring compliance with study protocols, and assisting with regulatory documentation. Freelancers may work with multiple organizations or research teams, offering flexibility and a diverse range of projects. This role requires strong organizational skills, attention to detail, and knowledge of clinical research regulations.

What skills and qualifications are needed to be a freelance clinical research assistant?

To succeed as a Freelance Clinical Research Assistant, you need a solid understanding of research methodologies, data collection, and regulatory compliance, typically supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like GCP (Good Clinical Practice) are highly valued. Excellent organizational skills, attention to detail, and effective communication enable you to manage multiple studies and collaborate with diverse teams. These abilities ensure accurate data management, adherence to protocols, and successful project outcomes in the dynamic field of clinical research.

What unique challenges do freelance clinical research assistants face compared to full-time positions?

Freelance Clinical Research Assistants often need to adapt quickly to new protocols, study teams, and sponsor expectations with each project. Unlike full-time roles, freelancers are responsible for managing their own schedules, securing contracts, and ensuring compliance across diverse research sites. Additionally, establishing clear communication with multiple stakeholders and staying updated on regulatory changes are crucial for success. However, this role offers flexibility and the opportunity to work on a variety of studies, enhancing your experience and professional network.

What is the difference between Freelance Clinical Research Assistant vs Clinical Research Coordinator?

AspectFreelance Clinical Research AssistantClinical Research Coordinator
CredentialsTypically requires a degree in health sciences or related field; certifications like CCRP are a plusRequires a degree in health sciences, nursing, or related field; often holds certifications like CCRP or CCRP
Work EnvironmentIndependent, project-based, often remote or on-site at research sitesEmployed by research institutions or sponsors, primarily on-site at clinical trial locations
Employer & Industry UsageFreelance roles are common in industry and contract research organizationsFull-time or part-time staff in hospitals, research centers, or pharmaceutical companies

The main difference is that a Freelance Clinical Research Assistant works independently on specific projects, often remotely, while a Clinical Research Coordinator is typically employed full-time by an organization to oversee clinical trials. Both roles require similar credentials and work in the same industry, but their employment structure and work environment differ.

What job categories do people searching Freelance Clinical Research Assistant jobs in Rochester, MI look for?

The top searched job categories for Freelance Clinical Research Assistant jobs in Rochester, MI are:

What cities near Rochester, MI are hiring for Freelance Clinical Research Assistant jobs?

Cities near Rochester, MI with the most Freelance Clinical Research Assistant job openings:

Freelance Clinical Research Assistant jobs near you

Clinic Research Coordinator I

Detroit, MI

DM Clinical Research
11 - 50 employees
Learn more about DM Clinical Researchexternal

$24 - $32/hr

Full-time

Re-posted 12 days ago

Job description

Clinic Research Coordinator I
The Clinical Research Coordinator I, will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. The CRC I will also ensure study enrollment meets or exceeds Sponsors' expectations. To ensure company goals are achieved on a timely basis.
Duties amp; Responsibilities:
  • Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
  • Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
    • a. Sponsor-provided and IRB-approved Protocol Training
    • b. All relevant Protocol Amendments Training
    • c. Any study-specific Manuals Training, as applicable
    • d. Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
  • Conducting study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.
  • Adherence to ALCOA-C Standards with all the relevant clinical trial documentation.
  • Completing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
  • Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
  • Demonstrated understanding and implementation of Laboratory Manuals and protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration and laboratory kit inventory, under the direction of the Site/Study Management Team, for assigned protocols.
  • Liaising with Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives, under the direction of the Site/Study Management Team, for assigned protocols.
  • Submitting required administrative paperwork per company timelines.
  • Participating in subject recruitment and retention efforts.
  • Engaging with Research Participants and understanding their concerns.
  • Any other matters, as assigned by management.

Knowledge amp; Experience:
Education:
  • High School Diploma or equivalent required
  • Bachelor's degree a plus
  • Foreign Medical Graduates preferred
Experience:
  • At least one years of experience as a CRC, preferably with practice coordinating industry-sponsored vaccines in a private setting.
  • At least two years of experience as a research assistant, data coordinator, laboratory personnel, or equivalent experience in a clinical research setting
Credentials:
  • ACRP or equivalent certification is preferred
  • Registered Medical Assistant certification or equivalent is preferred
  • Knowledge and Skills:
  • Be an energetic, go-getter who is detail-oriented and can multi-task.
  • Be goals-driven while continuously maintaining quality.
  • Bilingual in Spanish is preferred

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