Senior Clinical Research Coordinator

This role is ideal for highly qualified individuals holding an M.Sc. in Clinical Research/Life Sciences or Pharm.D/M.Pharm degrees, coupled with 3-4 years of experience as a Clinical Trial Coordinator. Candidates must possess ICH-GCP Certification and strong computer skills for data management. This position is perfect for those seeking project-based, contractual work within a leading medical research institution and who are comfortable with a consolidated remuneration structure.

Candidates seeking permanent government employment with standard benefits (such as Provident Fund, HRA, CCA, LTA, or Medical Claim) should not apply, as this is a purely temporary and contractual position. Individuals unable to join by the urgent deadline of 15-09-2026 are also not suitable. Those without specific clinical trial coordination experience and ICH-GCP certification will not meet the essential criteria.

Working at JIPMER, a prominent central government institution for medical education and research, offers significant prestige and invaluable experience. Although contractual, this role provides exposure to a multi-center, international, randomized, double-blind, placebo-controlled clinical trial, enhancing a professional's research profile and opening doors to future high-level research opportunities.