Description

You will support clinical research and development by drafting, negotiating, and advising on clinical and research-related agreements. Partnering with Clinical Development, Clinical Operations, and Legal teams, you will enable efficient and compliant execution of clinical programs in a fast-paced biotech environment.

Requirements

• Juris Doctor (JD) from an accredited law school and active license to practice law
• 10+ years of relevant legal experience with strong focus on clinical development or life sciences contracts
• Demonstrated experience negotiating CTAs and CRO agreements in biotech, pharmaceutical, or law firm setting
• Strong understanding of clinical trial operations and regulatory frameworks
• Excellent drafting, negotiation, and communication skills

Responsibilities

• Draft, review, and negotiate clinical development agreements including CTAs, site agreements, CRO, SMO, vendor, and consulting agreements
• Advise internal stakeholders on legal, regulatory, and risk considerations for clinical development activities
• Support contracting strategy and process improvements to streamline clinical contracting workflows
• Partner with Clinical Operations and Legal to identify and mitigate contractual and operational risks
• Manage multiple agreements simultaneously while meeting clinical timelines