Key Responsibilities
- Coordinate day-to-day clinical trial activities at assigned study sites
- Required 50 %to 55% Travelling
- Assist Principal Investigators in study conduct and documentation
- Screen, recruit, and follow up with study participants
- Ensure compliance with protocol, ICH-GCP guidelines, and regulatory requirements
- Maintain study documentation, source documents, and case report forms (CRFs)
- Coordinate site initiation, monitoring, and close-out visits
- Communicate with sponsors, CROs, ethics committees, and hospital staff
- Track patient visits, adverse events, and study timelines
- Ensure proper informed consent process is followed
- Maintain accurate clinical trial data and reports
- Travel frequently to hospitals, clinics, and research sites across Kolkata and nearby regions
- Support audit and inspection readiness activities

Required Qualifications




- Master of Science in Clinical Research Life Sciences, Pharmacy, Biotechnology, or related field
- Certification in Clinical Research is preferred
- 1-4 years of experience in clinical research or clinical trial coordination
- Knowledge of ICH-GCP, regulatory guidelines, and clinical trial processes
- Strong communication and coordination skills
- Ability to manage multiple sites and travel extensively

Preferred Skills
- Good documentation and reporting skills
- Familiarity with EDC systems and MS Office
- Strong interpersonal and organizational abilities
- Problem-solving and time management skills
- Ability to work independently and in a team workplace

Pay: ₹20,000.00 - ₹45,000.00 per month

Work Location: Hybrid remote in Kolkata, West Bengal

📌 Clinical Research Coordinator (Kolkata)
🏢 Simbi Labs India
📍 Kolkata