Clinical Research Coordinator
Ingenious Healthcare
Pune
11.2023
- Verifying that source documents and other trial records are accurate, complete, kept up-to-date, and maintained
- Checking the accuracy and completeness of the case report forms (CRF) entries, source documents, and other trial-related records against each
- Verifying proper IP storage and accurate drug information
- Compilation of study-related documents
- Co-ordinate with Ethics Committee activities for submission and Ensure the fulfillment of all inclusions and exclusions
- Compile and update the trial master
- SAE reporting within time
- Manage the clinical trial material with accountability
- Coordinate all lab-related activities
- Schedule the subject visit as per protocol
- Resolving queries raised by the CDM team.
