Counsel, Clinical Contracting

Highlights

• Lead end-to-end negotiation of global site agreements for late-phase studies.
• Partner with Clinical Ops, Finance, Regulatory and CROs to drive timely execution.
• Shape contracting templates and workflows to speed study startup.

What they offer

• Annual bonus
• Equity compensation
• Competitive benefits package

Ideal candidate

Proactive, detail-oriented attorney who thrives in fast-paced collaborative environments and enjoys hands-on negotiation to keep late-phase clinical studies moving efficiently.

Requirements

• 5+ years of relevant experience in clinical contracting within biotechnology, pharmaceutical, or CRO environment
• Deep working knowledge of clinical site contracts and regulatory support documents
• Proven experience negotiating directly with clinical sites, academic institutions and/or investigators
• Ability to redline and finalize contracts efficiently and independently
• Demonstrated ability to manage high-volume contracting workflows under tight timelines
• Excellent interpersonal and communication skills with ability to build cross-functional relationships
• JD from accredited law school and admitted to practice in at least one US jurisdiction