Beam Therapeutics Jobs in United States

We are building a best‑in‑class Field Medical organization as a natural next step in the growth of our Medical Affairs organization at Beam therapeutics This Director (or Associate Director) level MSL will own a defined US territory with primary responsibility in sickle cell dise ...

We are seeking an experienced Program Manager to lead our innovative next-generation gene editing programs. · ...

· Responsible for the statistical strategy for one or more clinical programs/studies and providing oversight of CRO biometrics deliverablesSupport clinical development team to enable robust study design and execution with a focus on innovative and efficient quantitative decision ...

As an experienced Program Manager, you will play a critical role in achieving outcomes for our innovative next-generation gene editing programs. · Drive the BEAM-302 program team by partnering closely with the Program Lead and cross-functional program team members to manage all o ...

We are seeking an experienced Process and Cleaning Validation subject matter expert to provide validation support for development of the process and cleaning validation programs. · ...

Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Bea ...

Overview · Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabi ...

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We are seeking a highly skilled Technical Lead to own and advance our portfolio of Clinical applications. · ...

· Act as lead writer for clinical regulatory documents. · Plan and lead document development working with cross-functional colleagues. · ...

Beam Therapeutics is transitioning to a commercial stage company. · Key Responsibilities: · Responsible for Clinical Supplies Planning · Work with cross function team members to create packaging strategies · Provide technical expertise for clinical study protocolsPrior investigat ...

· Design and implement robust ETL processes to integrate data from diverse sources while ensuring data quality and Strong experience in Boomi development to create, test, and deploy integrations. · ...

A leading biotechnology company in Virginia seeks a Director (or Associate Director) of Field Medical Affairs. This role involves developing territory strategies, managing key accounts in sickle cell disease, and collaborating cross-functionally to prepare for product launches. C ...

A biotechnology company in Cambridge is seeking an experienced professional for a key role in Health Economics and Outcomes Research. Ideal candidates will have a master's degree, at least 10 years of relevant experience in observational research, and a proven track record in dru ...

Overview · Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabi ...

Job Title · Beam Therapeutics seeks a Senior Director to lead Market Access Strategy from Cambridge. Key responsibilities include developing and executing market access plans, building relationships with payers, and optimizing reimbursement strategies. · Responsibilities: · • · P ...

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The Medical Director of Pharmacovigilance will provide clinical/scientific/PV expertise to lead a full range of core medical safety activities including the development and oversight of benefit-risk strategies, risk management, and safety surveillance activities in support of Bea ...

· Participates in statistical programming activities on clinical studies and oversees CROs to generate analysis data sets and tables listings figures needed for clinical study reports regulatory submissions. · ...

The Sr. Director Clinical Quality Assurance will lead the Quality organization and be responsible for the overall GCP strategy. They will manage audits and inspections, implement quality management systems and lead a high-performing team. · Audit Strategy: Design deliver execute ...