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Study Start Up Associate I

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About the role

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Location: Cologne, Germany
 
Study Start Up Associate I role within ICON:
 
Selected 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 in Germany
 
To succeed you will need:
 
A high school diploma or local equivalent, Bachelor’s Degree preferably in life sciences will ensure your familiarity with regulatory guidelines and industry knowledge. Minimum of 1 year of experience or understanding of clinical study start up requirements and activities.
 
What’s Next?
 
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.
 
 
ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.

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