Are you looking for a Clinical Research Coordinator job in Kolkata? C-TrialPro is hiring a full-time CRC to support clinical trials in compliance with ICH-GCP guidelines. If you have a life sciences or pharmacy background and 1+ years of experience, apply now!
📌 Job Details
- Position: Clinical Research Coordinator (CRC)
- Location: Kolkata (On-site)
- Job Type: Full-time
- Experience: 1+ years (Preferred)
- Qualification: B.Sc/M.Sc in Life Sciences, B.Pharm/M.Pharm, or related field
📋 Job Description
As a Clinical Research Coordinator at C-TrialPro, you will:
✔ Coordinate daily clinical trial activities at the site.
✔ Recruit, screen, and enroll eligible study participants.
✔ Maintain eCRFs/CRFs and ensure accurate data entry.
✔ Liaise with sponsors, CROs, and ethics committees.
✔ Ensure compliance with study protocols, SOPs, and regulatory guidelines.
✔ Manage trial documentation and site files.
✅ Requirements
- Bachelor’s/Master’s degree in Life Sciences, Pharmacy, or related fields.
- Prior CRC or clinical research experience (1+ years preferred).
- Strong knowledge of ICH-GCP, clinical trial processes, and regulatory requirements.
- Excellent communication, organizational, and teamwork skills.
💡 Why Join C-TrialPro?
🔹 Work with leading biopharma sponsors on cutting-edge trials.
🔹 Growth-oriented work environment with learning opportunities.
🔹 Competitive salary + benefits.
🏢 About C-TrialPro
C-TrialPro is a clinical research organization (CRO) dedicated to advancing clinical trials with GCP-compliant processes. Visit ctrialpro.in for more details.
📩 How to Apply
Interested candidates can “Easy Apply” on LinkedIn or send their resume to [company email/contact].