Beam Therapeutics Job Trends

Beam is looking for a highlymotivated Engineer/Senior Engineerto join our growingManufacturing Sciences & Technology (MS&T)team.TheMS&T Engineerwillbe responsible forsupportingprocesstechnology transfersand GMP manufacturing atthe Beam Durham facility.Support includestechnical support and subject matterexpertiseforbulk drug substance and bulk drug productGMPclinical,PPQ, and commercialmanufacturing.This rolesupports the execution of the CMC program strategythrough strong collaborationand partnershipwithcross-functional team membersinProcess Development (PD), Analytical Researchand Development (ARD), Manufacturing, Supply Chain, Quality Control, and Quality Assurance. Responsibilities Supports MS&T activities related to mRNA and LNP programs Supports the technology transfer andimplementationof mRNAandLNPGMPmanufacturing processes, collaborates with sending and receiving site cross-functional team members Supportsbulk drug substance and bulk...

Beam is seeking a Manager Regulatory Affairs to progress a broad portfolio of advanced genetic medicines in a fast paced and dynamic biotech environment. The person will be responsible for supporting the development and implementation of the global regulatory strategy for Beam’s programs. Responsibilities In partnership and under guidance from the Regulatory Lead, drive the development of global regulatory strategy for Beam’s portfolio of advanced genetic medicines and ensure integration of regulatory tactics that support the broader corporate strategy. Incorporate evolving global regulatory requirements and guidance's with respect to gene editing and gene therapy, rare disease, orphan indications, breakthrough treatments...

Beam is looking for a highly talented and motivated Senior Manager, Statistical Programming, to join our growing Statistical Programming team in the Biometrics department. The senior manager will be responsible for developing and maintaining statistical programming functions within a therapeutic area to support various clinical studies and submissions to ensure successful execution for Beam’s clinical programs. In this role, you will work with the lead of statistical programming to develop statistical programming strategies and timelines. You will manage CROs, oversee programming activities and provide timely support to the cross-functional teams on statistical programming matters according to the project strategies and...

Beam is seeking an experienced and motivated Clinical Trial Manager (CTM) to join our growing Clinical Operations team. In this role, you will serve as the operational lead - driving timelines, fostering collaboration, and ensuring the successful execution of clinical trials. The CTM will oversee day-to-day activities throughout the clinical trial lifecycle. Key responsibilities include managing start-up, conduct, and close-out activities in alignment with industry and corporate standards within ICH/GCP Guidelines. Responsibilities Have the skillset and experience to manage all project team activities related study start up, conduct and close out activities. Work with Outsourcing and Contracts Management to ensure...

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 disease (SCD) and shared accountability across the Beam pipeline, including Alpha‑1 antitrypsin deficiency (Alpha‑1) and glycogen storage disease 1a (GSD). You will architect territory strategy, onboard priority treatment centers, engage KOLs and HCPs, generate actionable insights, and drive pre‑commercial launch readiness in close collaboration with cross‑functional partners. Responsibilities Develop and execute territory strategy map treatment centers, referral...

Beam is looking for a highly energetic and motivated Associate Director/Director, Patient Advocacy and Centricity to join our growing team. This individual will be responsible for leading patient advocacy efforts across no less than 2 programs and help to ensure our core focus on patients here at Beam. This role is responsible for developing and supporting our patient advocacy strategy. The successful candidate will have an ability to represent the patient voice at Beam, educate externally on Beam’s clinical development programs, work well cross-functionally, and problem solve. Responsibilities Engage and partner with patient advocacy organizations, key opinion leaders, policy makers,...

Beam is looking for a highly energetic Data Analytics and Integration Specialist to join our growing IT team. The Data Analytics and Integration Specialist will be responsible for designing, building, and maintaining integration solutions using Boomi AtomSphere platform. The role ensures seamless data flow between cloud and on-premise systems, supporting enterprise applications and business processes. The candidate will be heavily involved in data migration and integration efforts, particularly using Boomi, SAP, LabVantage LIMS, MES systems and Amazon Redshift Data Warehousing. Responsibilities ETL Development & Data Integration - Design and implement robust ETL (Extract, Transform, Load) processes to integrate data from...

Beam is seeking a highly talented and motivated AD/Director to join our growing Medical Writing team. The AD/Director will be responsible for creating, authoring, and leading the management of key documents for regulatory filings and clinical studies, such as clinical protocols and amendments, clinical study reports, investigator’s brochures, safety and efficacy summaries, and other documents required for regulatory submissions. Working across functions such as clinical operations, regulatory affairs, medical, biostatistics, and pharmacovigilance, this role will represent Medical Writing on study teams and will report to the VP of Medical Writing. Responsibilities Act as lead writer for clinical regulatory documents for...