Manager Regulatory Affairs
Beam Therapeutics(1 month ago)
About this role
The Manager, Regulatory Affairs will support advancement of Beam’s portfolio of advanced genetic medicines by developing and implementing global regulatory strategies. This role partners with the Regulatory Lead and cross-functional teams to ensure programs meet evolving global regulatory requirements and progress toward clinical and commercial goals. The position contributes to regulatory planning, submission preparation, and interactions with health authorities in a fast-paced biotech environment.
Required Skills
- Regulatory Strategy
- Global Regulations
- Regulatory Submissions
- Document Authoring
- Project Management
- Cross Functional
- Agency Interactions
- Communication
Qualifications
- BS in Medical or Scientific Field
- MS
- PharmD
- PhD
- MD
About Beam Therapeutics
beamtx.comBeam Therapeutics is a clinical-stage biotechnology company based in Cambridge, MA, pioneering precision genetic medicines using its proprietary base editing platform to make precise single‑base DNA changes without creating double‑strand breaks. The company advances both in vivo and ex vivo programs across hematology, rare genetic diseases, and oncology, moving several candidates toward clinical development. Beam combines engineered editors, delivery technologies, and extensive safety profiling to create durable, potentially one‑time treatments and partners with academic and industry collaborators to accelerate translation.
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