Position details
| Vacancy id | VAC-52602 |
|---|---|
| Job title | VAC-52602 Pharmacovigilance _National Consultant |
| Location | Kabul |
| Apply by | 12-Apr-2026 |
| Start date | 01-May-2026 |
| Duration | 3 months |
| Number of vacancies | 1 |
| Qualification |
Advanced degree in Pharmacy or public health (essential). Master's degree in degree in regulatory or pharmacy (desirable). |
| Sector experience |
Minimum of five year/s of demonstrable relevant experience in pharmacy (essential). |
| Geographical experience |
Minimum of five year/s of experience in Afghanistan (essential). |
| Languages |
Fluent in English (essential). Fluent in Dari (essential). Fluent in Pashto (essential). |
| CTG overview |
CTG was established in 2006, almost 20 years ago, in Afghanistan. We currently operate in 35 countries and have approximately 11,500 staff members committed to good! But do you know who we are? And what do we do? We provide tailored Human Resources and Staffing Solutions that support critical global initiatives across Humanitarian and Development sectors, and are now strategically foraying into new industries, including Construction, Energy, and IT, with a focus on high-risk regions. Here’s a list of services we offer: Visit www.ctg.org to find out more. |
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| Overview of position |
The Afghanistan Food and Drug Authority (AFDA), as the national regulatory authority, is responsible for ensuring the quality, safety, and efficacy of medicines, medical devices, healthcare products, and food. Despite important progress, Afghanistan’s regulatory system continues to face challenges, including limited technical capacity, high dependence on imported products, inconsistent adherence to quality standards, and evolving systems for product registration, inspections, licensing, and market surveillance. Strengthening AFDA’s regulatory functions in alignment with our client norms and standards is essential to protect public health, prevent substandard and falsified products, and support the country’s broader goals for health system resilience and universal health coverage. To advance these priorities, AFDA is implementing regulatory reforms guided by our client Global Benchmarking Tool (GBT), which provides a structured framework for assessing regulatory maturity and developing Institutional Development Plans (IDPs). To accelerate progress, specialized technical support is required to strengthen GBT implementation. Despite important progress in strengthening regulatory functions, Afghanistan continues to face challenges related the national pharmacovigilance system that requires further development to ensure the systematic detection, reporting, analysis, and prevention of adverse events associated with medicines and other health products. As effective pharmacovigilance systems are critical for identifying safety signals, improving the safe use of medicines, and protecting patients from adverse drug reactions and substandard or falsified products. Strengthening pharmacovigilance capacity will also support better regulatory decision-making and improve public confidence in health products available in the country. To address these priorities, AFDA is implementing regulatory reforms guided by our client Global Benchmarking Tool (GBT), which provides a structured framework for assessing regulatory system maturity and developing Institutional Development Plans (IDPs). Strengthening pharmacovigilance functions is a key component of these reforms. However, achieving this objective requires specialized technical expertise to support the implementation of GBT recommendations, improve adverse event reporting mechanisms, strengthen regulatory information systems, and enhance institutional capacity. Engaging an international consultant will provide targeted technical support, hands-on mentoring, and capacity-building to AFDA staff and relevant stakeholders. This support will contribute to establishing a more proactive and sustainable pharmacovigilance system that aligns with our client standards and international best practices, ultimately strengthening the protection of public health in Afghanistan. |
| Role objectives |
Purpose of the consultancy To strengthen the national pharmacovigilance system in Afghanistan by conducting a comprehensive assessment of institutional and operational gaps, establishing a proactive and standardized adverse event reporting and data management mechanism, supporting the implementation of Institutional Development Plans (IDPs) under our client Global Benchmarking Tool, updating national pharmacovigilance regulatory frameworks in line with international standards, and building sustainable capacity among AFDA staff and relevant stakeholders. Output: To strengthen the national pharmacovigilance system by identification of system gaps, establishment of a structured reporting mechanism for adverse events, implementation of pharmacovigilance-related GBT Institutional Development Plans, updated regulatory frameworks, and improved capacity of AFDA staff and key stakeholders Tasks 1. Review the existing pharmacovigilance framework, including legal, institutional, and operational components; conduct a baseline assessment; identify gaps; and develop a roadmap to strengthen the national pharmacovigilance system. 2. Design and implement a design and pilot a standardized PV reporting mechanism for selected hospitals, clinics, and private sector facilities, including the development of tools for data storage, analysis, and interpretation. 3. Facilitate the implementation of our client Global Benchmarking Tool (GBT) Institutional Development Plans (IDPs) on pharmacovigilance, monitor progress against agreed indicators, and provide periodic updates to AFDA and our client. 4. Develop or revise national pharmacovigilance policies, guidelines, and standard operating procedures (SOPs) to ensure alignment with our client recommendations and international best practices. 5. Plan and conduct training programs and workshops to strengthen the capacity of AFDA staff, health facility focal points, and other relevant stakeholders in pharmacovigilance reporting and system management. Deliverables: Deliverable 1: A comprehensive assessment report detailing key gaps and proposed strategies for strengthening the pharmacovigilance system, along with an implementation progress report on our client GBT Institutional Development Plans (IDPs) related to pharmacovigilance and surveillance. Deliverable 2: A functional and standardized pharmacovigilance data collection and reporting mechanism established across selected health facilities. Deliverable 3: Updated national pharmacovigilance policy, guidelines, and SOPs developed and submitted for approval. Qualifications and experience: 1. Essential: Advanced degree in Pharmacy or public health 2. Desirable: Specialization/Master’s degree in regulatory or pharmacy 3. Essential: Minimum five years’ experience in pharmacovigilance and medicine safety Skills / Technical skills and knowledge: - Excellent interpersonal and communication skills. - High sense of responsibility and strong organizational skills with ability to work under pressure. - Advanced computer literacy (Word, Excel, Power point, etc.) Language requirements: - Advanced knowledge of Pashtu and Dari - Excellent knowledge of English |
| Project reporting |
Our client Technical Officer-HSD |
| Key competencies |
To be determined |
| Team management |
To be determined |
| Further information |
Our client has zero tolerance for sexual misconduct, inaction against it and any form of retaliation against victims/survivors or bystanders who disclose, report, or participate in an investigation. Parallel to technical competence, recruitment, selection and hiring decisions will give due emphasis to assessing candidates value congruence, thorough background checks and reference check processes. This will ensure children and vulnerable adults are safeguarded from abusers and that abusers are prevented from joining our client Afghanistan office. Please report any concerning information regarding sexual exploitation and abuse by our client workforce and partners to our client office of Internal Oversight services at [email protected] Our client is a smoke free environment. |
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Disclaimer:
· At no stage of the recruitment process will CTG ask candidates for a fee. This includes during the application stage, interview, assessment and training. · CTG has a zero tolerance to Sexual Exploitation and Abuse (SEA) which is outlined in its Code of Conduct. Protection from SEA is everyone’s responsibility · CTG encourages all candidates applying for this advertisement to ensure that their candidate profile is up to date with up to date experience / education / contact details, as this will help you being considered further in your application for this role. |
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