Clinical Research Coordinator I

• 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.

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