Ritu Chahar

Background

About Ritu Chahar

Experienced Pharmacovigilance and Drug Safety professional with 5+ years in ICSR processing, MedDRA coding, and ADR reporting, primarily within the pharmaceutical industry. I hold a Master’s in Pharmacy and have worked on global safety databases in compliance with ICH-GCP and regulatory guidelines. Currently working as an Administrative Analyst in a Canadian GMP-certified lab, I support quality documentation and regulatory alignment — building transferable skills relevant to Health Canada compliance. Previously worked with BMO as a CSR, gaining strong communication and documentation abilities in a regulated Canadian environment. I’m actively upgrading my skills with certifications in Pharmacovigilance, MedDRA, Canadian Regulatory Affairs, and GCP. I’m seeking remote opportunities in: • Pharmacovigilance / Drug Safety • Regulatory Affairs • Medical Writing / Quality Documentation Let’s connect if you’re hiring in pharma, biotech, CROs, or healthcare regulatory spaces!