Pharmacovigilance Associate

clinstinct clinical research

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 SOPs
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)
Ensure patients referring physician receives notification of patients participation in
studies as requested by the patient
Meet with patient for each visit and maintain accessibility to discuss any
questions/concerns regarding the study
Dispense study medication in a professional and accountable manner following protocol
requirements