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Description
The Clinical Trial Associate is responsible for providing logistical support for Phase I and Phase II clinical studies.
- Develop, maintain and manage appropriate study documentation
- Initiate, maintain and reconcile Trial Master File
- Set up and maintain tracking systems and tools and report study metrics to support the clinical study
- Manage and track study-specific payments
Requirements:
- Bachelor s degree or equivalent undergraduate degree required (scientific or healthcare discipline preferred)
- 2+ years industry experience in equivalent role
- Working knowledge of international regulatory and ICH GCP guidelines
