Study Start Up Associate I
Talent Acquisition Business Partner
- Full Service Division
About the role
This vacancy has now expired. Please click here to view live vacancies.
- 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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Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
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12/10/2025
Summary
Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.
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12/01/2025
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How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i
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Quality and Compliance for New Entrants: A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job
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