- The candidate must have at least 1-2 years experience in Phase 1 Phase 3 clinical trials
- He / She should be responsible for conducting clinical trials, getting CDA signed from investigator and subsequently filling Feasibility forms, maintaining documentation for the patients enrolled in clinical trial, counselling patients, assisting investigators in informed consent process, handling lab sample packaging and arranging shipments, making electronic data (e-CRF) entries along with source documents , analyzing and reporting protocol deviations, reporting AE or SAE if needed, etc
- The candidate should be good knowledge in concepts of Good Clinical Practices (GCP) and ICH Guidelines, MS office, Valuable Communication skill in English, Hindi , Assamese and Oriya ( as applicable for the respective locations )

Desired Qualification for the Candidate :

- B. Pharm / M. Pharm / B.Sc. (Bioscience) / M.Sc. in Biotechnology, Microbiology, Molecular Biology etc.

Disclaimer: This job posting & Location has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

📌 EXPERIENCED Clinical Research Coordinator (CRC) (Guwahati)
🏢 CliniMed LifeSciences
📍 Guwahati