Senior Manager, Regulatory Affairs
Rapport TherapeuticsBoston, Massachusetts, United States
Posted October 23, 2025
160000 - 180000 USD year
Full Time
About the Company
Rapport Therapeutics is a precision medicine company focused on treating neurological disorders by targeting disease-driving neurocircuits using receptor-associated proteins (RAPs). This approach aims to overcome the limitations of current neuromedicines, offering more effective and manageable treatments. Led by an experienced team with strong records in neuroscience and drug discovery, Rapport was founded by Third Rock Ventures and Johnson & Johnson Innovation-JJDC, Inc., and is headquartered in San Diego and Boston.
Job Description
Rapport Therapeutics is seeking a Senior Manager of Regulatory Affairs to lead the regulatory execution for global Phase 3 clinical trials of RAP-219. This role involves ensuring successful interactions with regulatory authorities, coordinating submissions, and staying updated with evolving guidelines. The ideal candidate is a detail-oriented professional with experience in the pharmaceutical or biotechnology industry. Rapport values scientific innovation, teamwork, and employee growth.
Requirements
- Bachelors degree in life sciences or related discipline
- 8+ years of experience in Regulatory Affairs within the pharmaceutical or biotechnology
- Proven experience with Global CTA submissions and IND maintenance
- Strong knowledge of regulatory guidelines and clinical trial regulations
- Proficient working with regulatory submission software
- Proactive, self-motivated, and able to work independently
Benefits
- Competitive benefits package
- Life spending account
- Commuting reimbursement
- Unlimited PTO
