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Clinical Research Associate
2 months ago
Cone Health is seeking a highly skilled Clinical Research Coordinator to join our team. As a Clinical Research Coordinator, you will play a critical role in the day-to-day clinical research process, working closely with study subjects and other research staff to collect, compile, document, and analyze clinical research data.
Key Responsibilities- Coordinate multiple clinical trials simultaneously, managing and organizing various research activities efficiently and ensuring optimal use of resources and timely execution of research protocols.
- Serve as study coordinator for pharmaceutical and/or device trials, successfully coordinating site initiation visits, monitoring visits, and close-out visits, and ensuring adherence to protocol guidelines and regulatory requirements.
- Complete clinical tasks, such as electrocardiogram (ECG), pulmonary function tests (PFT), phlebotomy, drug administration, etc., when not prohibited by state or licensing board requirements under the supervision of the principal investigator.
- Complete documentation in the electronic health/medical record (EMR) system to securely maintain patient health records.
- Collect data from various sources, including patient charts, medical records, interviews, and diagnostic tests, and prepare comprehensive documentation, ensuring the accurate and reliable analysis of research data.
- Support the regulatory process in the submission of study protocols, consent forms, and recruiting materials to the Institutional Review Board and the department for approval, facilitating the regulatory compliance necessary for research projects in the hospital.
- Assess patients for protocol eligibility, ensuring the appropriate selection of participants for clinical trials, thereby enhancing the accuracy and validity of research outcomes.
- EDUCATION:
- Required: Bachelor's degree OR Associate's Degree (with 2 yrs experience) OR Healthcare/Health-related certification, e.g., EMT, Pharm Tech, Rad Tech, etc. (with 4 yrs experience)
- EXPERIENCE:
- Required: 4 Years (education and/or experience)
- LICENSURE/CERTIFICATION/REGISTRY/LISTING:
- Preferred: Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) certification
