Clinical Research Coordinator
Comtrust Charitable Trust Eye Hospital
Telichery
01.2024 - 04.2024
- Assisted in the coordination and administration of clinical trials.
- Collected and analyzed data to support research objectives.
- Maintained accurate and detailed records of clinical trial activities.
- Communicated effectively with research participants and team members.
- Assisted in preparing periodic reports summarizing progress of clinical studies.
- 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 .
- Developed case report forms for data collection at investigational sites.
- Reviewed CRFs for completeness and accuracy before database entry.
- Monitored patient safety during clinical trials according to established guidelines.
- Facilitated resolution of protocol deviations or violations reported by sites or detected through monitoring activities.
