Counsel, Clinical Contracting

📋 Description

• Lead the end-to-end review, negotiation, and finalization of a high volume of global clinical site
• Draft, review, and negotiate a wide range of clinical research-related agreements and documents
• Serve as key liaison between internal stakeholders and external partners (including CROs and
• Maintain tracking systems and manage document flow across internal platforms and with CRO partners
• Flag risks, non-standard contract terms, or deviations from approved templates
• Suggest improvements to templates, fallback language, workflows, and tracking systems

🎯 Requirements

• 5+ years of relevant experience in clinical contracting within a biotechnology, pharmaceutical, or
• Deep working knowledge of clinical site contracts and regulatory support documents
• Proven experience negotiating directly with clinical sites, academic institutions, and/or
• Ability to redline and finalize contracts efficiently and independently
• Demonstrated ability to manage high-volume contracting workflows under tight timelines
• Proven ability to manage high-volume workflows with minimal supervision

🎁 Benefits

• Annual bonus
• Equity compensation
• Competitive benefits package