Clinical Research Associate

Responsibilities: ‎Monitor clinical trial sites to ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements ‎Conduct Site Qualification Visits (SQV), Site Initiation Visits (SIV), Monitoring Visits (IMV), and Close-Out Visits (COV) ‎Perform Source Data Verification (SDV) and ensure data accuracy and integrity ‎Maintain Trial Master File (TMF / eTMF) documentation to ensure inspection readiness ‎Track protocol deviations, adverse events, and study-related issues ‎Support investigator training and site readiness activities ‎Collaborate with investigators, site coordinators, and clinical operations teams ‎Prepare monitoring reports and follow-up documentation Requirements : ‎Degree in Health Sciences, Medicine, Pharmacy, Nursing, or related field ‎Minimum 2–4 years of experience in clinical research or clinical trial monitoring ‎Strong understanding of ICH-GCP guidelines and clinical trial processes ‎Experience with site monitoring and regulatory...