clinstinct clinical research Bhubaneswar, Odisha

Overview

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

Skills / Roles I hire for

Pharmacovigilance Associate

We are currently hiring 1 job(s)

Pharmacovigilance Associate

clinstinct clinical research

  • Experience 0 - 1 yrs
  • Location Bhubaneswar
Pharmacovigilance Associate
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