Vidya r Purohit

I am an aspiring Clinical Trial Coordinator with a Bachelor of Pharmacy degree, driven by a passion for clinical research and quality assurance. My hands-on experience in production and pharmacovigilance has equipped me with a comprehensive understanding of regulatory guidelines and Good Clinical Practice (GCP) standards. I am eager to contribute to Metta Clinical Research by supporting high-quality clinical trials and ensuring regulatory compliance.

During my industrial training at Meyer Vitabiotics, I completed over 150 hours in the Production and Quality Control departments, gaining practical experience in manufacturing processes and compliance audits. As a pharmacist at Hari Medical, I managed an inventory of over 500 medicines, ensuring strict adherence to regulatory standards while assisting in adverse event monitoring and providing patient counseling. My strong organizational and analytical skills enable me to maintain precise documentation and compliance in all my endeavors.