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Mohammad F.

Pharmacovigilance Associate 0.2 yrs experience

Lucknow, Uttar Pradesh · Profile MFLU0TNK08XP

Experience0.2 yrs experience
EducationM.Pharm
LocationLucknow
Notice period—
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Profile summary

M.Pharm graduate (2026) and Pharmacovigilance-certified fresher with hands-on training in end-to-end ICSR case processing: case intake and triage, duplicate check, MedDRA coding, narrative writing, seriousness, expectedness and causality assessment (WHO-UMC, Naranjo), and regulatory reporting (E2B(R3), CIOMS, MedWatch) in the Argus safety database. Working knowledge of ICH-GCP, GVP modules, SUSAR reporting timelines and signal detection. Detail-oriented, with strong scientific documentation skills from research and industry training. Seeking a Pharmacovigilance Associate / Drug Safety Associate role to support patient safety and regulatory compliance.

Key skills

ICSR Case Intake & TriageDuplicate CheckData EntryNarrative WritingMedDRA Coding (LLT/PT/SOC)Quality CheckFollow-up QueriesLiterature ScreeningCausality Assessment (WHO-UMCNaranjo)AE/SAE/SUSAR ReportingE2B(R3)

Certifications

  • Pharmacovigilance (3-Month Course)
  • Pharmify & Payaam Vohra Classes
  • July 2026
  • Trained in ICSR case processing: intake, MedDRA coding, narrative writing, seriousness/expectedness and causality assessment.
  • Practised case entry, E2B(R3)/CIOMS reporting, signal detection and quality checks using the Argus safety database.
  • Clinical Research & Clinical Data Management (3-Month Course)
  • Covered ICH-GCP, clinical trial phases, protocol development, CDM, EDC systems and data validation.
  • Nov 2025
  • Feb 2024
  • April 2024
  • ACADEMIC RESEARCH PROJECT
  • 2025 – 2026