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Sr Study Start Up Associate

058474

About the role

This vacancy has now expired. Please click here to view live vacancies.

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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