Job Summary

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.

Qualification & Specifications:

MBBS,BDS,BHMS,BAMS,BSMS,PHARMACYB.Sc/M.Sc (Life Sciences / Biology / Bio Chemistry / Micro Biology / Nursing / Bio Technology), B.P.T, B.E BIOMEDIAL, B.Tech (Biotechnology/Bio Chemistry).

2025 -2026 passed out

Responsibilities:

- 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.

For more details contact

Kowshika - HR

(phone hidden)

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