Assist in setting up, monitoring, and closing clinical trial sites
Ensure that clinical trials are conducted according to protocol, GCP, ICH guidelines, and local regulatory requirements
Perform regular site visits (if applicable) to ensure compliance and data accuracy
Support in the collection and review of essential documents
Communicate with clinical trial sites, sponsors, and internal teams
Assist in preparing study-related documentation and reports
Maintain and track clinical trial supplies
Job Types: Full-time, Permanent, Fresher
Pay: ?22,743.24 - ?35,294.44 per month
Benefits:
Paid sick time
Provident Fund
Work Location: In person
MNCJobsIndia.com will not be responsible for any payment made to a third-party. All Terms of Use are applicable.