Senior Regulatory Affairs Consultant
Job Summary
To support a growing international pharmaceutical company, the contract Senior Regulatory Affairs Consultant will define regulatory strategies, lead Health Authority interactions, and provide strategic guidance within an active clinical program.
Key responsibilities
- Define and critically review the regulatory strategy for specific clinical development programs
- Lead and support interactions with Health Authorities, including the FDA, EMA, and MHRA
- Prepare and review meeting requests, briefing books, and agency meeting materials
Required qualifications
- 10-15+ years of hands-on Regulatory Affairs experience
- Strong track record of direct Health Authority interactions, particularly with the FDA, EMA, and MHRA
- Experience developing and reviewing global regulatory strategies
- Strong understanding of clinical development and scientific principles
- Ability to work independently and make sound regulatory judgments
Complete Job Description
The complete job description is available to members. Premium membership includes:
Full access to 41,964 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.
