Clinical Research Coordinator
1 week ago
Designation : Clinical Research Coordinator
Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.
Working closely with the PI ,CRC participates in an integral way in the informed consent process by communicating with the potential study subjects about protocol. Possesses a thorough knowledge of the informed consent process as well as a thorough understanding of the study protocol in order to be able to answer all questions pertaining to the study posed during the informed consent process.
Coordinates approval of new study aggrements and contracts.
Coordinates and attends sponsor Site Selection visits, Routine monitoring visits, and study close out visits.
Responds to data clarification requests in a timely manner.
Coordinates with PIs and departments to help ensure that clinical research and related activities are performed in accordance with protocol , SOP,GCP and applicable regulatory requirement.
7.Maintains subjects screening logs and protocol deviation logs.
8.Maintains excel sheet, tracking updates to database of all subjects enrolled on clinical trials.
Coordinates and Facilitates monitoring and auditing visits.
Collaborates with PI and institution to respond to any Audit findings and implement approved recommendations.
Establishes and organizes study files, including but not limited .
Location - Kolkata
Full Time , ON site
Only Freshers can apply
Qualifications required: BSc,Msc, Bpharm
Immediate Joining.
Interested candidates send resume in mail id
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