Open to opportunities

Mohammed Afzal

@mohammedafzal1

I process drug safety cases, author regulatory reports, and strengthen pharmacovigilance compliance across global safety systems.

India

Message

What I'm looking for

I'm looking to contribute my pharmacovigilance, medical writing, and regulatory safety reporting experience in a role focused on high-quality, compliant safety deliverables, cross-functional collaboration, and continued growth in global drug safety.

At IQVIA, I processed adverse drug reaction reports and Individual Case Safety Reports end to end, from intake and triage through medical coding, assessment, quality control, and regulatory submission. I also authored PSUR/PBRERs, PADERs, DSURs, Annual Reports/ACOs, and Risk Management Plans while supporting signal management, literature screening, reconciliation, audits, CAPA, and SOP improvements.

I'm a registered pharmacist who combines patient-focused medication knowledge with hands-on experience in Argus Safety, Aris G LSMV, and Veeva Vault Safety. I enjoy delivering accurate safety work under regulatory timelines, mentoring team members, and helping maintain inspection readiness across FDA, EMA, CDSCO, ICH-GCP, and GVP requirements.

Experience

Work history, roles, and key accomplishments

Current

Pharmacist

Current

Jan Aushadhi Pharmacy

Apr 2025 - Present (1 year 4 months)

Reviewed prescriptions for errors, drug interactions, and correct dosage; ensured accurate labeling and dispensing instructions. Counseled patients on safe medication use and managed drug stock and storage.

Reviewing Prescriptions Patient Counseling Inventory Management Regulatory Compliance

Operation Specialist 1 - Pharmacovigilance

IQVIA

May 2021 - Apr 2025 (3 years 11 months)

Processed adverse drug reaction reports and Individual Case Safety Reports (ICSRs) end to end using Argus, Aris G LSMV, and Veeva Vault Safety platforms. Authored aggregate safety reports (PSUR/PBRER, PADER, DSUR) and supported signal detection and risk management activities.