Contract Length: 3-6 months supporting cardiac device study
Must have experience ding blood draws
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 Good 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
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