Clinical Research Analyst
Job Summary
To support the Human Research Protection Program, the full-time Clinical Research Analyst will analyze and review regulatory submissions related to human subjects research, serve as a resource for researchers, and ensure compliance with institutional and regulatory requirements while working remotely.
Key responsibilities
- Analyze and review full-board and expedited reviews, adverse events, and protocol modifications
- Provide support to Institutional Review Board (IRB) members and serve as a liaison between the IRB and researchers
- Ensure compliance with regulatory and institutional requirements for human subjects research
Required qualifications
- 4 years of experience in a health-related field or research, or an equivalent combination of education and experience
- 3 years of experience with IRB, regulatory, or research processes
Complete Job Description
The complete job description is available to members. Premium membership includes:
Full access to 43,976 remote jobs from human-vetted companies, updated daily
Resume Builder - AI-powered tool to craft, enhance, and tailor your resume to a specific job
Twice-monthly live group coaching and the full Remote Career Center
20% member discount on Career Services
Backed by a 30-day money-back guarantee
Company Company Name
Headquarters Headquarters
Founded Founded
Website
Wikipedia Wikipedia URL
BBB URL BBB URL
The company description is available to members. Go Premium for full access to every job and company profile in our remote jobs database, backed by a 30-day money-back guarantee.
