Brief Description:
The medical person will be responsible for providing medical input on key study documents (e.g., Medical Monitoring Plan, ICF, eCRFs, etc.), as well as monitoring subject eligibility and safety. The medical person will also provide input on the medical interpretation of safety data in clinical trials.
Essential Functions
Job Types: Full-time, Contract
Schedule:
License/Certification:
Willingness to travel:
Work Location: Remote
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