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Clinical Trial Manager (on - Site)
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Full-time
- Works cross-functionally with other Guardant Health departments (such as Bioinformatics, Clinical Operations, Regulatory Affairs, Client Services, etc.)
- Assess feasibility of study timelines and pharmaceutical partner requirements.
- Finalize Data Transfer Agreements (DTA) and Data Transfer Specifications (DTS) as needed.
- Responsible for training of investigative site staff and providing ongoing educational assistance to ensure compliance with study protocol and applicable regulatory requirements.
- 2+ years direct trial management experience, preferably including clinical team management.
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