Clinical Research Co-ordinator
Indus Diabetic & Obesity Centre
Bhayander West
09.2024 - Current
- Developed and maintained accurate and timely study databases.
- Provided guidance on Good Clinical Practice regulations and other applicable regulatory standards.
- Coordinated investigator meetings, conference calls, and site initiation visits as needed.
- Reviewed CRFs for completeness and accuracy before database entry.
- Maintained accurate up-to-date tracking logs for all aspects of clinical research activities including but not limited to adverse events, serious adverse events, concomitant medications, lab results .
- Kept patient care protocols and clinical trial operations in compliance.
- Compiled trial related documents into a master file as required by sponsor or regulatory agency.
- Developed and maintained trial master files in accordance with GCP and ICH guidelines.
- Planned, organized and coordinated clinical trials in accordance with GCP and ICH guidelines.
- Operated equipment and machinery according to safety guidelines.
