Location: Kolkata (On-site)
Job Type: Full-time
Experience: 1.5-2 years (Up to 2 years preferred)
Qualification
- B.Pharm / M.Pharm
- B.Sc. (Hons.) Biotechnology
- M.Sc. (Life Sciences/Biotechnology or related field)
- B.Tech Biotechnology
- Other Life Science graduates may apply
Key Responsibilities
- Coordinate day-to-day clinical trial activities at study sites.
- Schedule participant visits and act as a liaison between study participants and the Principal Investigator (PI).
- Assist in the informed consent process and ensure protocol compliance.
- Maintain study documentation, regulatory files, and participant tracking logs.
- Complete and update Case Report Forms (CRFs/eCRFs) accurately and on time.
- Maintain study databases and Excel trackers.
- Coordinate study start-up activities, contracts, and approvals.
- Work closely with investigators, sponsors, monitors, and the clinical research team.
- Ensure compliance with ICH-GCP guidelines, study protocols, and applicable regulations.
Required Skills
- Good communication and organizational skills.
- Proficiency in Microsoft Office (especially Excel).
- Attention to detail and documentation.
- Basic knowledge of Clinical Research and GCP is preferred.
Benefits
- Provident Fund (PF)
- ESIC
- Gratuity
- Paid Leave
- Career Growth Opportunities
Work Schedule: Day Shift
Work Location: On-site, Kolkata
Pay: ₹12,000.00 - ₹30,000.00 per month
Benefits:
Work Location: In person
