Headline

Patient Safety Associate II | 2+ Years Pharmacovigilance | Argus ICSR | Clinical Trial Safety | Patient-Oriented Programs.

About

Pharmacovigilance professional with experience in end-to-end processing of Individual Case Safety Reports (ICSRs) across Post-Marketing (POP) and Clinical Trial (CT) projects. Experienced in case triage, data entry, and medical coding using MedDRA and WHO Drug Dictionary while ensuring compliance with global pharmacovigilance guidelines and timelines. Currently working as Patient Safety Associate II, handling complex safety cases including SUSARs and contributing to high-quality safety data management. Also experienced in mentoring junior team members and supporting efficient case processing while maintaining strong data quality and regulatory compliance. Committed to continuous learning and contributing to patient safety through effective pharmacovigilance practices.

Location

Hisar

Work experience

Patient Safety Associate II at paraxel international india pvt ltd, Feb 2026 - Present · 6 mos, Mohali district, India, CT (Clinical Trials): Performing end-to-end ICSR case processing including triage, data entry, and medical coding using MedDRA and WHO Drug Dictionary. Handling SUSAR cases while ensuring compliance with global pharmacovigilance timelines and mentoring junior team members to maintain data quality. ●POP (Post-Marketing Pharmacovigilance): Handled end-to-end ICSR case processing including triage, data entry, medical coding (MedDRA/WHO-DD), and ensured compliance with global safety timelines.

Drug Safety Associate at paraxel international india pvt ltd, Dec 2023 - Mar 2026 · 2 yrs 4 mos, Mohali

Drug Safety Associate Trainee at ACI - A Pharmacovigilance Training Management Company, May 2023 - Apr 2024 · 1 yr, Mohali district, India

Education

Master's degree, Pharmacology, CHANDIGARH UNIVERSITY

Guru Jambheshwar University