Clinical Research Coordinator I
About The Position
The Clinical Research Coordinator I will coordinate and conduct the day-to-day operations of TRIAD ongoing studies in cardiovascular diseases. The Clinical Research Coordinator I is required to have an 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 Clinical Research Coordinator screens, enrolls and follows study patients, ensuring protocol compliance, and effective monitoring of clinical trial subjects. The Clinical Research Coordinator I is also responsible for all data and source documentation, adverse event reporting and maintenance of complete regulatory files.
Requirements
- In-depth knowledge of protocol requirements.
- In-depth knowledge of good clinical practices as set forth by federal regulations.
Responsibilities
- Coordinate and conduct day-to-day operations of TRIAD ongoing studies in cardiovascular diseases.
- Act as a liaison between the patient, investigator, Institutional Review Board and sponsor.
- Screen, enroll and follow study patients, ensuring protocol compliance.
- Monitor clinical trial subjects effectively.
- Responsible for all data and source documentation.
- Responsible for adverse event reporting.
- Responsible for maintenance of complete regulatory files.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
