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Clinical Research Compliance Jobs (NOW HIRING)

Honorhealth

Specialist - Research Compliance

Reviews Clinical Trial Management (CTMS) builds for accuracy against contract and budget at onset ... Miscellaneous projects as assigned by the lead research compliance team members and director of ...

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How much do clinical research compliance jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for clinical research compliance in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

What is clinical research compliance?

Clinical research compliance refers to the set of processes and regulations that ensure clinical trials and research activities are conducted ethically, legally, and in accordance with regulatory standards. It involves adhering to guidelines set by agencies like the FDA, IRB, and Good Clinical Practice (GCP) standards. Compliance professionals help protect the rights and safety of research participants, ensure data integrity, and minimize risks for research institutions. Their work includes monitoring studies, training staff, and maintaining up-to-date documentation to meet all legal and ethical requirements.

What are the key skills and qualifications needed to thrive in clinical research compliance?

To excel in Clinical Research Compliance, you need a solid understanding of clinical research regulations, Good Clinical Practice (GCP), and relevant ethical guidelines, often supported by a degree in life sciences or a related field. Familiarity with regulatory systems such as FDA, ICH guidelines, and electronic data capture (EDC) platforms, as well as certifications like CCRA or CCRC, is highly valuable. Strong attention to detail, critical thinking, and effective communication skills set standout professionals apart in this role. These abilities are crucial to ensure research integrity, patient safety, and adherence to regulatory standards in clinical studies.

What are the main challenges faced by professionals in clinical research compliance, and how can they prepare for them?

Professionals in Clinical Research Compliance often encounter the challenge of staying current with evolving regulations and ensuring that research protocols are consistently aligned with ethical and legal standards. They must navigate complex documentation processes, monitor for protocol deviations, and collaborate closely with research teams to implement corrective actions. Preparation involves continuous education, strong organizational skills, and developing effective communication channels with investigators and regulatory bodies. Proactively building a network within compliance and research communities also helps in sharing best practices and staying informed about industry changes.

What is the difference between Clinical Research Compliance vs Clinical Research Coordinator?

AspectClinical Research ComplianceClinical Research Coordinator
Required CredentialsRegulatory certifications, knowledge of GCP, FDA, ICH guidelinesEducational background in health sciences, sometimes certifications in research
Work EnvironmentRegulatory departments, compliance offices, research institutionsClinical sites, hospitals, research facilities
Employer & Industry UsagePharmaceutical companies, CROs, research institutionsHospitals, clinics, research centers
Common Search & ComparisonFocuses on regulatory adherence and policyFocuses on patient recruitment, data collection, and study coordination

While Clinical Research Compliance professionals ensure that studies adhere to regulations and guidelines, Clinical Research Coordinators manage the day-to-day operations of clinical trials. Both roles are essential in the research process but focus on different aspects of clinical research.

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Clinical Research Compliance jobs near you
Infographic showing various Clinical Research Compliance job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, and 4% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Clinical Research Compliance Specialist

MIT Human Resources

Cambridge, MA

Full-time

Re-posted 2 days ago

Job description

CLINICAL RESEARCH COMPLIANCE SPECIALIST, Vice President for Research, to ensure compliance with federal, state, and local policies, and guidelines related to research protocols involving human subjects at MIT on behalf of the Committee on the Use of Humans as Experimental Subjects (COUHES). The primary responsibility is to ensure that research protocols are clinically sound, ethical, and aligns with best practices, minimizing participant risk while ensuring standard of care, clear informed consent, and appropriate recruitment and screening. Duties require on-campus presence to review study facilities and conditions. 

The full job description is available, here.

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About MIT Human Resources

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Our mission is to advance a vibrant and diverse work community where individuals and groups thrive and contribute to MIT's excellence. We offer Support, Services, and Programs to enhance your work life. We're here to help. MIT is committed to helping employees achieve a healthy balance between their careers and the full lives they lead off-campus. Explore all of MIT's Work & Life resources, including MyLife Services, which provides 24/7 access to a network of experts available to help with life’s challenges.

Industry

Human resource programs administration

Company size

1 - 10 Employees

Headquarters location

Cambridge, MA, US

Year founded

2014

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