Overview
This consultancy aims to support the Therapeutic Information and Pharmacovigilance Centre (TIPC) in developing and implementing Institutional Development Plans (IDPs) to advance Namibia's pharmacovigilance maturity level.
Key Responsibilities
- Review the GBT self-benchmarking assessment report and identified gaps
- Prioritize interventions in the Institutional Development Plans (IDPs) for relevant TIPC regulatory functions
- Provide technical assistance, guidance, and mentoring to staff for intervention implementation
- Compile monthly reports on progress made
- Participate in resource mobilization including proposal development
- Undertake additional tasks as assigned by the supervisor
Required Experience
- At least 5 years of progressively responsible experience in pharmacovigilance, medicine safety, regulatory systems strengthening, or related public health fields, including direct experience supporting national pharmacovigilance systems in low- and middle-income countries.
- Proven experience working with the WHO Global Benchmarking Tool (GBT)
- Experience in mentoring staff
- Experience in strategic planning and institutional development
- Knowledge of Namibia's health sector context will be a distinct advantage.
- Experience in working on strengthening medicines regulation and pharmacovigilance in Southern Africa Development Community (SADC) countries is desirable.
- Experience working with Ministries of Health, medicines regulatory authorities, public health programs, development partners, and healthcare facilities is desirable.
Qualifications
- Advanced degree (Masters level) in pharmacy, public health, regulatory science, or related field.
- PhD in pharmacy with a strong focus on pharmacovigilance is desirable.