Senior Director, Global Site Contracts

Role: Senior Director, Global Site Contracts leading worldwide clinical site contracting activities to enable efficient and compliant trial initiation and conduct. Responsibilities include developing global contracting strategy, overseeing all contract lifecycle stages (CTAs, investigator agreements, MSAs, etc.), driving process improvements, ensuring regulatory compliance, and managing cross-functional stakeholder relationships. The role involves strategic governance, risk mitigation in study startup, vendor performance management, and operational excellence initiatives. It requires supervising a global team and fostering a culture of accountability and continuous improvement. Qualifications include extensive experience in clinical trial contracting or site management, strong leadership skills, and knowledge of GxP, ICH-GCP, and regulatory standards relevant to global clinical trials. High-value biopharma specifics encompass supporting oncology trials, managing contracts across multiple regions, and collaborating with Clinical Operations, Legal, Compliance, Finance, and CROs. The role may involve strategic oversight of study startup risk and vendor relationships, with a focus on high-quality, timely, and compliant contract execution to support clinical development milestones.