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Manager Regulatory Affairs at Beam Therapeutics - ApplyBlast

Manager Regulatory Affairs

Beam Therapeutics

10 months ago

4.1 on Glassdoor

Cambridge, MA

Onsite

Full Time

Manager

2 applicants

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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.

Skills

Qualifications

BS in Medical or Scientific FieldMSPharmDPhDMD

About Beam Therapeutics

beamtx.com

Headquarters

Cambridge, Massachusetts, United States

Company Size

501-1000 employees

Founded

2017

View Profile

Beam 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.