Senior Regulatory Affairs Specialist
Job Summary
Independently managing essential regulatory documentation for clinical studies, the full-time Senior Regulatory Affairs Specialist will assist project teams, perform compliance assessments, and oversee submissions to regulatory bodies while working remotely.
Key responsibilities
- Assist and advise project teams on regulatory requirements for clinical studies
- Perform compliance assessments and document findings, notifying Project Managers as necessary
- Compile and review regulatory documentation for submission to IRBs, ECs, and other regulatory bodies
Required qualifications
- Associate's or Bachelor's degree in an allied health field such as nursing, pharmacy, or health science, or equivalent relevant experience
- At least 5 years of relevant pharmaceutical, site, or CRO regulatory experience
Complete Job Description
The complete job description is available to members. Premium membership includes:
Full access to 41,015 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
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.
