beamtherapeutics
Associate Director, Contracts
At a Glance
- Location
- Cambridge, Massachusetts, United States
- Experience
- 3–7 years
- Posted
- 2026-03-17T12:56:08-04:00
Key Requirements
Domain Knowledge
- Automation
- Biotech
- Clinical
- Education
- Healthcare
- Legal
- Manufacturing
- Medical
- Pharmaceutical
- Regulatory
Requirements
strongly preferred, with 3–7 years of contracts experience in biotech, pharma, or a life sciences or legal department.
Demonstrated ability to independently manage the full contract lifecycle, drafting, negotiating, and executing a high-volume, diverse portfolio of agreements including CTAs, MSAs, Research & Collaboration, and Commercial Supply/Manufacturing contracts.
Experience supporting Commercial and Medical Affairs functions, with familiarity advising on Advisory Boards, Sponsorships, Grants, and other healthcare-facing engagements.
Working knowledge of healthcare compliance frameworks, including HCP engagement practices, fair market value standards, and applicable regulatory requirements.
Familiarity with global clinical trial site contracting processes and experience reviewing informed consent forms and related clinical documentation.
Hands-on experience with contract lifecycle management (CLM) platforms, with an interest in or track record of contributing to workflow automation, template development, and process improvement initiatives.
Responsibilities
Beam Therapeutics seeks a business-focused Associate Director, Contracts / Contracts Attorney to manage a high volume of agreements across clinical, research, manufacturing, quality, commercial, and corporate functions.
Reporting to the Director of Contracts & Compliance, this role provides pragmatic, risk-balanced legal support, partners closely with cross-functional stakeholders, and helps strengthen contracting infrastructure as the company advances toward commercial-stage operations.
Draft, review, negotiate, and manage a broad range of agreements, including Clinical Trial Agreements, Master Services Agreements, Consulting, Confidentiality, Research & Collaboration, and Commercial Supply/Manufacturing Agreements.
Review and advise on clinical informed consent forms and related documentation.
Support compliance contracting processes, including healthcare professional engagement documentation and fair market value validation.
Partner with Compliance and cross-functional teams to implement and administer approval workflows supporting Commercial, Legal, and Medical Affairs activities.