Beam Therapeutics - United States, Research and Development

Lead the strategic BEAM-302 gene therapy program as a key operational leader in Cambridge. This senior role requires 12+ years in biotech, with expertise in cross-functional program management for cell/gene therapies. You will drive integration across clinical, CMC, regulatory, and manufacturing ...

Join Beam as an Associate Director/Director of Biostatistics in Cambridge, US. Lead statistical strategy and oversight for clinical trials in rare disease and gene/cell therapy. Utilize your PhD and 7+ years' industry experience, including regulatory submissions (NDA/BLA) and advanced methods lik...

Join Beam's mRNA Science team for a summer 2026 internship in Cambridge, USA. You will produce and screen novel mRNA designs using IVT reactions and analytical assays. This role is ideal for a detail-oriented student in biological sciences seeking hands-on lab experience in cutting-edge gene edit...

Join Beam's LNP Process Development Team as a Process Engineering Intern in Cambridge, USA. This summer 2026 role involves scale-up activities, process characterization, and data analysis for next-gen formulations. Ideal candidates are pursuing a BS/MS in a related field and are eager to support ...

Join Beam's Analytical R&D team in Cambridge as a CryoEM Image Analysis Intern. Develop state-of-the-art image processing pipelines to support novel gene editing therapies. Ideal candidates have a background in image processing and are enrolled in Biophysics, Bioinformatics, or a related field. C...

Lead global regulatory strategy for cutting-edge genetic medicines at Beam. This Cambridge-based role requires 8+ years of Regulatory Affairs experience, including IND/CTA/BLA submissions. You will drive strategy, author submissions, and interface with Health Authorities for a dynamic portfolio.

Lead regulatory labeling for innovative genetic medicines at Beam. This Cambridge-based role requires 6+ years in Regulatory Affairs, Advertising, Labeling, and Promotion. You will create core labeling documents and lead negotiations with global health authorities.

Lead clinical development for innovative in-vivo base editing programs targeting genetic metabolic disorders. As Medical Director, you will design trials, provide medical monitoring, and support global regulatory strategy. This Cambridge-based role requires an MD with 15+ years' experience, inclu...

Lead regulatory medical writing for a growing gene therapy leader. Craft key documents like protocols, CSRs, and IBs for hematology programs. This Cambridge-based role requires 12+ years' pharma/biotech experience and offers mentorship opportunities.

Join Beam's Clinical Operations team as a Clinical Trial Manager in Cambridge, US. Drive timelines and execution for clinical trials, leveraging 8+ years of biotech/pharma experience. A background in Phase I, rare disease, or cell & gene therapy is highly desirable. This role offers impactful wor...