Clinical Trial Intern
- Assisted in coordinating clinical trial activities, including patient recruitment and screening and documentation ( ICF and CRF).
- Supported data collection and entry into electronic data capture systems .
- Collaborated with clinical research coordinators to monitor trial progress and compliance with Good Clinical Practice (GCP).
- Assisted in the preparation of regulatory documents and ethics committee submissions.
- Gained practical knowledge of clinical trial phases, protocol development, and regulatory requirements.