Are you ready to run global oncology studies at pace and turn rigorous science into operational reality for patients sooner? In this role, you will orchestrate complex, multi-country trials from protocol through Clinical Study Report, ensuring quality and compliance while unblocking the path to decisive data.

Accountabilities

• Study Document Leadership: Drive the development, updates and amendments of core study documents, ensuring template and version compliance from start-up through closeout.
• Country Start-up and Submissions: Lead country-specific agreements, confidentiality agreements and clinical trial applications to enable rapid site activation across multiple geographies.
• Vendor Strategy and Oversight: Set up and manage third-party vendors, assess statements of work and budgets, oversee change orders, and ensure partners deliver to quality, timeline and cost.
• Data Delivery Enablement: Provide input to data management documents...