Draft, review, and negotiate a wide range of agreements, including:
Master Services Agreements (MSAs)
Statements of Work (SOWs)
Clinical Trial Agreements (CTAs)
Non-Disclosure Agreements (NDAs) and Confidential Disclosure Agreements (CDAs)
Consulting Agreements
Provide legal support for global transactions and cross-border collaborations
Advise on and support engagements with Clinical Research Organizations (CROs)
Handle R&D-related legal work, including:
Pre-clinical research agreements
Sponsored research agreements (e.g., industry–academic collaborations)
Material Transfer Agreements (MTAs)
Support licensing and collaboration agreements within the life sciences space
Partner with business stakeholders, including business development and licensing (BD&L) teams, on strategic and operational initiatives
Contribute to structuring and negotiating research collaborations and related transactions

J.D. and active bar membership in good standing
Experience in the pharmaceutical, biotech, medical device, or health system sectors (a blend is preferred)
Demonstrated experience in at least one of the following priority areas:
Global transactional experience
Working with Clinical Research Organizations (CROs)
R&D legal work, including pre-clinical and sponsored research
Familiarity with intellectual property transactions in the life sciences space
Experience supporting licensing, collaboration, and research agreements
Strong drafting, negotiation, and stakeholder management skills

Clinical Trial Counsel, Commercial & R&D – Pharma / Life Sciences

Key skills