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Clinical Research Coordinator II
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Full-time
- Clinical Research Coordinator II
- Assists with and adheres to Institutional Review Board (IRB) renewal, modification, and approved protocols.
- Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process.
- Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines.
- May involve other regulatory/Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation.
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