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Sr Study Start Up Associate

058474

About the role

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This is an exciting opportunity to join ICON

Senior Study Start Up Associate

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
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