Open to CRCs or CRNs

Therapeutic area: Cardiac

POSITION SUMMARY

The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Clinical Research Manager, the Principal Investigator and the Medical Director. The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials. The CRC will perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study specific protocols.

Duties and Responsibilities

Administratively and clinically manage an average of six to eight clinical trials Adhere to Research SOP’s

Adhere to Valuable Clinical Practices and the study protocols





Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials

Discuss study protocols with patients and verify the informed consent documentation Provide patient with written communication of their participation (i.e. copy of the signed informed consent)

Dispense study medication in a professional and accountable manner following protocol requirements

Perform ECGs and obtain vital signs of patients

Schedule all patient research visits and procedures consistent with protocol requirements

📌 Clinical Research Coordinator (Cambridge)
🏢 Medix™
📍 Cambridge