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Ngetwa S. — Mid-Level Pharmacovigilance Specialist from Tanzania

Ngetwa S.

Mid-Level Pharmacovigilance Specialist

Tanzania 1-2 years
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Languages
English
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About

Stephen E. is a dedicated and versatile Pharmacist with specialized expertise in pharmacovigilance, adverse event case processing, regulatory reporting, and clinical safety data management. At the University of Dar es Salaam Hospital (UDSM Hospital), he coordinates and manages institutional pharmacovigilance activities, monitoring drug safety signals and overseeing medication safety surveillance to safeguard patient outcomes. His proficiency in Safety Data Management Systems is evidenced by his experience managing Individual Case Safety Reports within VigiFlow and ensuring compliance with GVP, ICH, and WHO guidelines. Stephen also excels in signal detection, risk assessment, and literature-based safety surveillance, directly contributing to regional risk evaluation and mitigation strategies. His experience as an intern pharmacist involved regulatory reporting and patient safety measures, ensuring accurate entry of adverse drug reactions into local and national safety databases. Stephen's commitment to quality assurance is demonstrated through routine professional drug inspections across local pharmacies. Fluent in English and Kiswahili, he holds a degree from St John's University of Tanzania.

Experience

  • Pharmacist & Pharmacovigilance Focal Person

    University of Dar es salaam Hospital (UDSM Hospital) · 2025 — Present
    Manage and coordinate pharmacovigilance activities within the hospital, monitoring drug safety signals to ensure patient safety. Oversee medication safety surveillance, documenting drug-drug interactions, adverse drug reactions (ADRs), and medication errors.
  • Intern Pharmacist

    Tanzania medicine and medical device at Southern Highland Zone and Mbeya Regional Referral Hospital · 2023 — 2024
    Collected and documented adverse drug reactions as part of adverse event case processing, ensuring timely entry into safety databases. Verified data accuracy for Individual Case Safety Reports (ICSRs) within VigiFlow. Prepared and submitted safety reports to TMDA and WHO, adhering to regulatory timelines. Conducted data analysis for signal detection and risk assessment, supporting regional safety evaluations. Executed literature searches to identify global drug safety trends and drafted clinical documentation to support patient safety and regulatory compliance.

Skills & Expertise

Education

  • Tanzanian higher education degree
    St John’s University of Tanzania · — — 2023

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