Siva Prasad

I am a pharmacovigilance professional with over two years of hands-on experience in adverse event reporting, case processing, and quality review within global safety operations. I have worked on clinical trial and post-marketing case types and contributed to projects for major sponsors.

At IQVIA I improved patient safety by accurately reviewing, processing and following up adverse event reports, and I served as a Subject Matter Expert clearing queries and monitoring team quality and production. I have practical experience with ArisG, LSMV, ARGUS and i-Medidata Rave safety gateway processing.

My strengths include meticulous narrative writing, regulatory-compliant processes (ICH-GCP/PVP), and managing product quality complaints while meeting high productivity and quality targets. I was recognized with internal awards for excellence, including an Ovation Award and Best Employee of the Month for 97% quality and 115% productivity.

I am a quick learner and strong team player who works well under pressure and is proficient with Microsoft Office and pharmacovigilance regulatory and data management activities. I am seeking roles where I can continue to enhance patient safety and contribute to high-quality safety operations.