Pradnyaa Jadhav
Clinical Research Associate @Visshwa Solutions
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WORK HISTORY
Clinical Research Associate @Visshwa Solutions
Sangli, IN
Monitor clinical trials to ensure compliance with protocols, ICH-GCP guidelines, and regulatory requirements.•Perform site selection, initiation, routine monitoring, and close-out visits.•Ensure accurate documentation and maintenance of essential documents in Trial Master File (TMF).•Identify, document, and follow up on protocol deviations, adverse events (AEs), and serious adverse events (SAEs).•Ensure timely reporting of study progress and site status to project teams and sponsors.
EDUCATION
Bharati Vidyapeeth
Bharati Vidyapeeth college of pharmacy kolhapur
ABOUT PRADNYAA JADHAV
Passionate Clinical Research Associate (CRA) in clinical trial monitoring, regulatory compliance, and site management. I specialize in ensuring high-quality data collection, adherence to Good Clinical Practice (GCP) guidelines, and seamless coordination between sponsors, investigators, and regulatory authorities.Key expertise : Site initiation, monitoring Protocol compliance & regulatory submissions
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