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Clinical Trials Coordinator
2 months ago
Position Overview:
The Clinical Research Coordinator operates autonomously, managing the coordination of clinical studies. This includes evaluating potential participants for eligibility based on study protocols, explaining non-medical trial concepts, and facilitating the informed consent process.
Key Responsibilities:
- Ensure accurate and prompt documentation of source materials, data collection, and reporting, including timely responses to inquiries from sponsors.
- Compile and present comprehensive reports on each study, detailing protocol activities, participant enrollment statistics, workload metrics, and other relevant research data during regular staff meetings.
Strategic Planning:
- Develop and implement strategies aimed at enhancing patient enrollment, boosting operational efficiency, training staff, and identifying new research opportunities.
Compliance Assurance:
- Maintain adherence to all applicable federal and local regulations, including those set forth by the Food and Drug Administration (FDA) and local Institutional Review Boards (IRB).
