• Coordinate day-to-day clinical trial activities at the site
• Support investigators during patient screening, enrollment, and follow-up
• Maintain essential trial documents including ISF, CRFs, and study logs as per GCP
• Ensure compliance with ICH-GCP, SOPs, and regulatory guidelines
• Coordinate with sponsors, CROs, ethics committees, and study monitors
• Support study initiation, monitoring visits, and close-out activities
• Ensure accurate data collection and timely resolution of queries
• B.Pharm or M.Pharm (Pharmacology)
• Freshers or candidates with prior clinical research experience
• Knowledge of clinical research processes and GCP principles
• Strong documentation and communication skills
• Proficiency in Gujarati, Hindi, and English
• Willingness to work full-time at the Ahmedabad site
Nirmit Clinical Research is a clinical research organization focused on conducting ethical, high-quality clinical trials while providing hands-on training and growth opportunities for aspiring clinical research professionals.
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