Clinical Research Coordinator I
About the role
The Clinical Research Coordinator I will coordinate and conduct the day-to-day operations of TRIAD ongoing studies in cardiovascular diseases. This role requires in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations. As the primary resource for protocols, the Clinical Research Coordinator I acts as a liaison between the patient, investigator, Institutional Review Board, and sponsor.
The coordinator screens, enrolls, and follows study patients, ensuring protocol compliance and effective monitoring of clinical trial subjects. Responsibilities also include managing all data and source documentation, adverse event reporting, and maintenance of complete regulatory files.
Responsibilities
- Coordinate and conduct day-to-day operations of clinical studies in cardiovascular diseases.
- Act as a liaison between patients, investigators, Institutional Review Board, and sponsors.
- Screen, enroll, and follow study patients while ensuring protocol compliance.
- Monitor clinical trial subjects effectively.
- Manage all data and source documentation for studies.
- Report adverse events and maintain complete regulatory files.
Qualifications
- Minimum Qualification: Bachelor’s Degree in public health or other science area, or RN with current Louisiana licensure at the time of hire. Three years of clinical research experience in conducting research and clinical trials, including recruitment and coordinating research activities.
- Preferred Qualification: Master’s Degree in clinical research or public health. Certified Clinical Research Coordinator. Clinical research experience in cardiovascular disease, hypertension, and renal disease.
About Us
Tulane University is an equal opportunity educator and employer.