(Sr) Project Manager, Feasibility Site Activation

About the role

This is a highly visible position where you will take ownership of the Study Start-Up (SSU) strategy and execution—ensuring that sites are activated efficiently, regulatory pathways are navigated effectively, and studies are positioned for successful delivery from day one. You will work at the center of cross-functional collaboration, partnering with sponsors, internal teams, and sites worldwide to deliver start-up excellence at scale.

What you'll do

• Shape and execute Study Start-Up strategies across global, multi-country studies, ensuring alignment with timelines, scope, and sponsor expectations
• Lead the development and delivery of comprehensive Study Start-Up Plans, covering regulatory, ethics, and contract execution across all participating countries
• Drive end-to-end start-up activities from site identification through to IP release, maintaining momentum and accountability for key milestones
• Provide strategic input at Bid Defense and Kick-Off meetings, influencing study design and start-up feasibility from the outset
• Oversee regulatory and ethics submissions, ensuring high-quality, compliant, and timely approvals across regions

What you need

• Stakeholder management
• Clinical research
• Learning and development
• Process improvement