November 23, 2021
Full Time
Req Number: 
Under the supervision of a Clinical Research Supervisor or Principal Investigator (PI), the Assistant Clinical Research Coordinator  (Assistant CRC) will serve as a liaison between research participants and other faculty/study staff members to perform duties related to the support and coordination of clinical research studies.

The Assistant CRC will be responsible for support and coordination of various clinical research studies, including:
•    Study activation 
•    Participant recruitment, scheduling, and testing
•    Research and regulatory protocol management
•    Communication with all elements of a multi-level research network, interacting with sponsoring agencies and compliance and regulatory groups such as the Institutional Review Board (IRB), and other sponsor monitors 
•    Study coordination and operation, including scheduling of various exams and assessments for both in-person and remote participants
•    Discrete and professional patient interaction
•    Data collection and data management.
•    Coordination of clinical research with biomarker studies