Mohamed Moussa
@mohamedmoussa
I review drug safety cases and regulatory risk-management submissions for biological medicines.
EgyptWhat I'm looking for
At Oncopharm, I serve as Qualified Person for Pharmacovigilance, reviewing ICSRs, managing follow-ups and reconciliations, and maintaining RMPs, PSURs, PSMF, SOPs, and local safety documentation.
Previously, I managed the Egyptian Drug Authority's Biological Products Safety Unit, leading three professionals and assessing around 200 pharmacovigilance and biological safety files annually, including RMPs, PSURs, ICSRs, vaccines, biosimilars, and blood products. I'm seeking to deepen my end-to-end ICSR case-processing and international drug safety operations experience while applying my regulatory safety assessment background.
Experience
Work history, roles, and key accomplishments
Qualified Person for Pharmacovigilance (QPPV)
Oncopharm
Mar 2026 - Present (6 months)
Perform review and quality assessment of Individual Case Safety Reports (ICSRs), manage follow-up requests, and reconcile safety cases with MAH records. Review RMPs, PSURs, and maintain the PSMF, while supporting regulatory communication with the Egyptian Drug Authority.
Education
Degrees, certifications, and relevant coursework
Ain Shams University
Bachelor of Pharmaceutical Sciences, Pharmaceutical Sciences
2011 - 2016
Grade: Excellent with Honors – 90.4%
Bachelor of Pharmaceutical Sciences with honors, achieving a grade of 90.4%.
Tech stack
Software and tools used professionally
Availability
Location
EgyptAuthorized to work in
Job categories
Skills
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