Manager Site Start UP EUCTR

About the role

As Manager, Site Start-Up, EU Clinical Trials Regulation, you will lead the planning and delivery of Part II clinical trial applications through the Clinical Trials Information System.

What you'll do

• Build our future together
• Lead the planning and delivery of Part II clinical trial applications through the Clinical Trials Information System
• Connect Regulatory Affairs, Clinical Trial Management, Clinical Transparency, contract research organizations, and study sites to establish submission strategies
• Lead the planning and execution of European Union Clinical Trials Regulation Part II submissions throughout the study lifecycle
• Partner with Clinical Trial Management and Regulatory Affairs to define country allocation, submission strategy, breakthroughs, and timelines

What you need

• 7–13 yrs of experience
• PowerPoint
• Research
• Excel
• Clinical research
• Regulatory affairs
• Project management
• Any graduate

Good to have

• MS Project
• Compensation and benefits