Tushar Sharma

Background

About Tushar Sharma

As a Drug Safety Associate with 8+ months of ICSR experience and a Master’s degree in Pharmacovigilance & Clinical Research, I bring strong technical skills and a deep understanding of global PV processes. I'm well-versed in case triage, narrative writing, regulatory submissions, and confident with Argus Safety (IVP). I’ve also completed a 6-month internship in aggregate report writing (PSUR/PBRER), giving me hands-on exposure to safety data analysis and compliance documentation. I’m now actively seeking growth opportunities where I can contribute to end-to-end pharmacovigilance operations, including signal detection, aggregate reporting, and quality review. My goal is to align with a team that values ownership, skill enhancement, and global compliance. What I Bring: Strong command over ICSR workflows, Argus & (IVP) ICSR Case Triage & Submissions Fast learner, adaptable to evolving regulations Exposure to aggregate reports internship level (RMP, PBRER/PSUR/PADER) Solid knowledge of MedDRA, WHO-DD coding Professional communication & deadline discipline Willingness to go beyond job descriptions when needed I’m open to: Full-time PV roles (ICSR, QA, Aggregate, Literature) MNCs, CROs, and global regulatory environments On-site or hybrid positions across India Let’s connect if you’re hiring in pharmacovigilance — or feel free to refer me where I can add value.