We are looking for a candidate who is interested in developing a career in clinical research. The candidate will receive practical exposure to clinical trial processes, documentation, regulatory requirements, Positive Clinical Practice (GCP), and clinical research operations.
- Assist with clinical trial documentation and record maintenance.
- Support preparation and organization of essential trial documents.
- Learn clinical trial protocols and study procedures.
- Assist in maintaining Trial Master File (TMF) documentation.
- Coordinate with internal teams for study-related activities.
- Support data collection and basic clinical research activities.
- Follow GCP, SOPs, and applicable regulatory requirements.
Skills:
- Basic knowledge of clinical research concepts.
- Understanding of medical terminology.
- Good documentation and organizational skills.
- Willingness to learn clinical trial processes.