Study Start Up Associate I
3 tygodni temu
At ICON, we're committed to fostering an inclusive environment that drives innovation and excellence. As a Study Start Up Associate I, you'll play a crucial role in ensuring the successful activation of study sites. Your responsibilities will include performing routine essential document collection, review, and negotiation, as well as recruiting study sites and tracking clinical data. You'll also be responsible for setting up and maintaining study documents in application systems and forecasting submission/approval timelines. If you're a detail-oriented and organized individual with strong communication skills, we encourage you to apply.
Key Responsibilities:
- Perform routine essential document collection, review, and negotiation
- Recruit study sites and track clinical data
- Set up and maintain study documents in application systems
- Forecast submission/approval timelines and provide risk and contingency plans
What You Need:
- Polish and English language fluency
- German, French, Italian, Dutch languages an advantage
- Bachelor's degree or international equivalent (preferred life-sciences degree or be a licensed healthcare professional)
- Good spoken and written communication skills
- Strong collaborative and time management skills
Benefits of Working at ICON:
At ICON, we offer a range of benefits to support your well-being and work-life balance. These include competitive salary packages, health-related benefits, and retirement plans. We're committed to providing a workplace free of discrimination and harassment, and we welcome applications from diverse candidates. If you need a reasonable accommodation for any part of the application process, please let us know. We're an equal opportunity employer and are committed to providing a workplace that is inclusive and accessible to all.
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Study Start Up Associate I
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