Clinical Study Coordinator
- Coordinate clinical research projects in accordance with Code of Federal Regulations
- Provide technical and regulatory support to Principal Investigators
- Implement quality assurance measures to ensure compliance across physicians, patients, and clinicians
- Abstract relevant medical data from patient records
- Report adverse events to medical monitors, the FDA, and applicable governing bodies
- Coordinate external audits and monitoring visits; act as liaison between sponsor and institution
- Serve as a resource for departmental and system-wide initiatives
- Bachelor's degree in Clinical Research, Biology, Chemistry, Nursing, or related field
- Minimum 2 years of experience as a Clinical Study Coordinator
- SOCRA or ACRP certification preferred
- IATA certification preferred
- Cardiology and/or regulatory background is a plus
- Strong organizational, analytical, problem-solving, verbal, and written communication skills
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