Study Start up Associate I

This is an exciting opportunity to join ICON

To coordinate clinical trial start-up activities and serve as primary contact for investigators and research coordinators in corporate and public sponsored human clinical trials.

• Prepare, review contract negotiation with external sites in Germany, working to project deadline to finalise study contracts
• You will be collaborating with multiple internal and external teams to coordinate the contract templates and budgets throughout the timeframe
• Completing contract amendment activities
• Other study start up activities as required including: ethics submissions, creating submissions packages, amendments to study documentation according to country guidelines

Role Requirements

• Bachelor's Degree or local equivalent and/or appropriate experience from the Medical/science background and/or discipline
• Global clinical trials experience with awareness of global regulatory requirements for clinical site initiation documents