IRB Program Manager
Job Summary
Overseeing the development and compliance of clinical research trials, the full-time IRB Program Manager will manage regulatory guidance, coordinate IRB processes, and ensure adherence to federal and state regulations while working remotely.
Key responsibilities
- Coordinates review and approvals of research proposals to ensure compliance with IRB and regulatory requirements
- Interacts with governmental agencies and prepares for audits regarding research regulations
- Plans and implements training programs for IRB members and research staff on regulatory guidelines
Required qualifications
- Master's degree in a relevant field or equivalent experience
- Experience in clinical research and IRB processes
- Knowledge of federal regulations related to human subjects research
- Proven ability to provide regulatory and ethical guidance
- Experience in developing and implementing training programs
Complete Job Description
The complete job description is available to members. Premium membership includes:
Full access to 42,491 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
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.
