- 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
- 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
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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