Clinical Trials Coordinator

2 weeks ago


Fountain Valley, California, United States Medix™ Full time

Position Overview:
The Clinical Research Coordinator operates autonomously, overseeing the coordination of clinical studies. This includes the evaluation of potential participants for eligibility based on study protocols, conveying non-medical trial information, and facilitating the informed consent process.

Key Responsibilities:
- Ensure the accuracy and timeliness of source documentation, data collection, and reporting, including prompt responses to inquiries from sponsors.
- Compile and present comprehensive reports on each study, detailing protocol activities, enrollment data, workload, and other pertinent research information during regular staff meetings.

Strategic Planning:
- Develop and implement strategies aimed at enhancing patient enrollment, optimizing 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).



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