Clinical Research Coordinator

Skip to main content Clinical Research Coordinator Sova Health Gurugram, Haryana, India Apply Clinical Research Coordinator Sova Health Gurugram, Haryana, India 2 weeks ago 69 applicants See who Sova Health has hired for this role Apply Save Report this job Use AI to assess how you fit Get AI-powered advice on this job and more exclusive features. Am I a good fit for this job? Tailor my resume Sign in to access AI-powered advices Email or phone Password Show Forgot password? Sign in Sign in with Email or New to LinkedIn? Join now By clicking Continue to join or sign in, you agree to LinkedIn’s User Agreement, Privacy Policy, and Cookie Policy. Sign in to evaluate your skills Email or phone Password Show Forgot password? Sign in Sign in with Email or New to LinkedIn? Join now By clicking Continue to join or sign in, you agree to LinkedIn’s User Agreement, Privacy Policy, and Cookie Policy. Sign in to tailor your resume Email or phone Password Show Forgot password? Sign in Sign in with Email or New to LinkedIn? Join now By clicking Continue to join or sign in, you agree to LinkedIn’s User Agreement, Privacy Policy, and Cookie Policy. Designation: Clinical Research Coordinator (CRC)Location: Gurugram (Medanta)Reporting To: Principal Investigator / Clinical Research ManagerAbout The RoleWe are looking for a detail-oriented and proactive Clinical Research Coordinator (CRC) to support the successful execution of clinical trials while ensuring compliance with regulatory requirements, study protocols, and Good Clinical Practice (GCP) guidelines. The ideal candidate will coordinate study activities, maintain accurate documentation, collaborate with investigators and sponsors, and ensure the highest standards of participant safety and data integrity throughout the clinical research process.Key ResponsibilitiesCoordinate and conduct clinical trials in compliance with ICH-GCP guidelines, approved study protocols, SOPs, and applicable regulatory requirements. Support study start-up activities, including site preparation, participant recruitment, screening, enrolment, follow-up, and retention. Maintain complete and accurate study documentation, including source documents, Case Report Forms (CRFs), study logs, Site Master File (SMF), and Investigator Site File (ISF). Manage Investigational Product (IP) accountability, including receipt, storage, dispensing, reconciliation, shipment, and documentation....