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Clinical Research Associate 1
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- Responsible for providing Clinical Research support for all clinical trials.
- Under the direction of supervisor or designee, this position will serve as support for the clinical study team.
- Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to clinical research functions.
- Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials.
- Conduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions.
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