Consultant โ€“ Paediatric medicines Access

Tags: Environment
  • Added Date: Monday, 26 January 2026
  • Deadline Date: Monday, 09 February 2026
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Qualifications

Purpose of consultancyย  ย ย 

The purpose of this consultancy is to contributeย  to the design and implementation of a national framework to strengthen the paediatric medicines ecosystem in four ASEAN countries (Thailand, Indonesia, Malaysia and the Philippines), with the goal of improving access to safe and effective medicines for children with high-burden conditions.

Backgroundย ย 

Despite sustained efforts by Member States of the World Health Organization (WHO), civil society and other stakeholders, many countries are still facing multiple challenges in ensuring availability, affordability and rational use of quality-assured medicines that are adapted for children to prevent or treat high burden conditions. At the Seventy-seventh World Health Assembly, Member States re-committed to improving the health of children and have called on Member States, stakeholders and the WHO secretariat to enable access to safe, high-quality and age-appropriate essential medicines for children. They urged accelerating implementation of priority actions by promoting, supporting and financing investigation, development, manufacturing, registration and supply of age-appropriate, quality-controlled formulations of medicines for diseases that affect children.

The Global Accelerator for Paediatric Formulations (GAP-f) is a WHO Network launched in 2020 to advance access better paediatric medicines. It is a network of 30 organizations, that works across the life cycle of drug development, by bringing efficiency through enhanced coordination across stakeholders to prioritize, evaluate, develop and deliver better Paediatric medicines.

GAP-f is led by a Secretariat, which is responsible for developing and maintaining the GAP-f strategy, leading GAP-fโ€™s advocacy work, and overall operations of GAP-f. The Secretariat sits within WHOโ€™s Science for Health Department, and has a coordination function, liaising with around 30 external organizations as well as multiple technical departments within WHO. The GAP-f Secretariat supports the work of four working groups which are designed to gather GAP-f network members and leverage their expertise to address systemic barriers across the product life cycle. The working groups include prioritization, clinical research, product development and regulatory affairs, and product access and treatment delivery. The access and treatment delivery working group facilitates the work on the network to ensure that better formulations are effectively introduced and rapidly rolled out.

Building on collaborations with technical departments and ongoing work led by GAP-f partners, WHO is committed to enable end-to-end action on paediatric medicines innovation and access and utilise GAP-f crosscutting expertise to improve the paediatric medicines ecosystem for high-burden conditions. This work will start in Asia and focus on diseases highly prevalent in ASEAN countries (i.e. dengue, malaria, bacterial infections and non-communicable diseases). The collaboration with WHO will focus on documenting successful models for increasing access to optimal paediatric medicines and scale up those models across the region with a focus on 4 ASEAN countries (Malaysia, Thailand, Indonesia and the Philippines). In this work, we plan to collaborate with national programmes, national academic institutions and centres of excellence for child health across the region.

To this end, the WHO is seeking a short-term consultant (โ€œThe Consultantโ€) to provide technical and coordination and support to the design and implementation of a generic national framework to improve paediatric medicines ecosystem enabling better access to important safe effective medicines for high burden conditions affecting children in the ASEAN region. In doing so the candidate selected will engage and leverage support and expertise of the GAP-f Access and Treatment Delivery working group and work with national and regional WHO offices and technical experts from counterpart organizations and governments in Southeast Asia.

Deliverables

Task 1: Development and Implementation of a Customized Essential Paediatric Medicines Framework (4 ASEAN Countries)ย 

๐Ÿ“š ๐——๐—ถ๐˜€๐—ฐ๐—ผ๐˜ƒ๐—ฒ๐—ฟ ๐—›๐—ผ๐˜„ ๐˜๐—ผ ๐—š๐—ฒ๐˜ ๐—ฎ ๐—๐—ผ๐—ฏ ๐—ถ๐—ป ๐˜๐—ต๐—ฒ ๐—จ๐—ก ๐—ถ๐—ป ๐Ÿฎ๐Ÿฌ๐Ÿฎ๐Ÿฏ! ๐ŸŒ๐Ÿค ๐—ฅ๐—ฒ๐—ฎ๐—ฑ ๐—ผ๐˜‚๐—ฟ ๐—ก๐—˜๐—ช ๐—ฅ๐—ฒ๐—ฐ๐—ฟ๐˜‚๐—ถ๐˜๐—บ๐—ฒ๐—ป๐˜ ๐—š๐˜‚๐—ถ๐—ฑ๐—ฒ ๐˜๐—ผ ๐˜๐—ต๐—ฒ ๐—จ๐—ก ๐Ÿฎ๐Ÿฌ๐Ÿฎ๐Ÿฏ ๐˜„๐—ถ๐˜๐—ต ๐˜๐—ฒ๐˜€๐˜ ๐˜€๐—ฎ๐—บ๐—ฝ๐—น๐—ฒ๐˜€ ๐—ณ๐—ผ๐—ฟ ๐—จ๐—ก๐—›๐—–๐—ฅ, ๐—ช๐—™๐—ฃ, ๐—จ๐—ก๐—œ๐—–๐—˜๐—™, ๐—จ๐—ก๐——๐—ฆ๐—ฆ, ๐—จ๐—ก๐—™๐—ฃ๐—”, ๐—œ๐—ข๐—  ๐—ฎ๐—ป๐—ฑ ๐—ผ๐˜๐—ต๐—ฒ๐—ฟ๐˜€! ๐ŸŒ

โš ๏ธ ๐‚๐ก๐š๐ง๐ ๐ž ๐˜๐จ๐ฎ๐ซ ๐‹๐ข๐Ÿ๐ž ๐๐จ๐ฐ: ๐๐จ๐ฐ๐ž๐ซ๐Ÿ๐ฎ๐ฅ ๐“๐ž๐œ๐ก๐ง๐ข๐ช๐ฎ๐ž๐ฌ ๐ก๐จ๐ฐ ๐ญ๐จ ๐ ๐ž๐ญ ๐š ๐ฃ๐จ๐› ๐ข๐ง ๐ญ๐ก๐ž ๐”๐ง๐ข๐ญ๐ž๐ ๐๐š๐ญ๐ข๐จ๐ง๐ฌ ๐๐Ž๐–!

Final Bottleneck Analysis Tool โ€“ in collaboration with WHO at country, regional and global levels.Country-Specific Bottleneck Analysis Report documenting key challenges and barriers identified through stakeholder engagements.Stakeholder Consultation Summary - findings from national consultations, including identified gaps and proposed solutions.Customized National Frameworks (Draft & Final) โ€“ A tailored essential paediatric medicines framework for each of the four countries including implementation plan (with piloting) and monitoring and evaluation framework.Pilot Implementation Report โ€“ Documenting progress, lessons learned, and recommendations from piloting the framework.

Task 2: National Adoption & Adaptation of the Essential Medicines List for Children (EMLc)

Development of an EMLc 2025 Dissemination Strategy & Materials in the four ASEAN countries.
Expected by: March 2026Development of a priority disease mapping report โ€“ Identification of priority diseases per country based on local epidemiology and government priorities.Development of a comparative analysis of existing national EMLs against the 2025 EMLc, with recommendations for revision.Development of a Policy Gap Analysis Report โ€“ Assessment of policy gaps related to EMLc adoption and adaptation for priority diseases.

Development of a customized M&E Plan for Essential Paediatric Medicines including a framework to support future updates and impact assessment.

Task 3: Leveraging Global Platforms to Accelerate the Introduction of Novel Therapeutics for Paediatric Use

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Updated GAP-f Access & Delivery Toolkit โ€“ Revised version of toolkit incorporating best practices for accelerating paediatric therapeutic introductions.Development of training materials for capacity strengthening such as customized resources for virtual training sessions.Training Session Reports โ€“ documentation of sessions conducted, participant engagement, and key takeaways.

Task 4: Regional Collaboration for Strengthening the Paediatric Medicines Ecosystem.

Regional Stakeholder Engagement Report โ€“ Summary of regional challenges and opportunities identified.Regional Workshop Materials & Summary Reports โ€“ Agenda, presentations, key takeaways, and action items from discussions.Development of a regional roadmap for paediatric medicines ecosystem strengthening โ€“ A strategic framework based on pilot outcomes.Stakeholder Engagement Log โ€“ Documentation of ongoing engagements, opportunities, and shared actions.

Task 5: Coordination of GAP-fโ€™s Access and Delivery Working Group

Development of an Access & Delivery Working group workplan with defined objectives and milestones aligned with GAP-f Phase 3 strategy.Meeting & Webinar Reports โ€“ Documentation of discussions, outcomes, and action points from ad hoc meetings.Access & Delivery Working Group Engagement Summary โ€“ Detailing contributions and feedback from working group members on ASEAN initiatives.

Qualifications, experience, skills and languages

Educational Qualifications:ย  ย Essential:

University degree (Masterโ€™s level) in medical or social science.

Desirable: Advanced University degree (PhD level) in clinical epidemiology, public health, pharmacy or equivalent.ย 

Experienceย ย Essential:ย 

At least 5 years of relevant experience in managing and coordinating collaborative projects.

Experience with introduction and roll out of new medical health products .Desirable:

Experience providing technical and capacity-building support to government and development partners in Asia

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Experience and expertise in key aspects of pharmaceutical management, including national regulatory framework, procurement, and supply chain management

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Skills/KnowledgeEssential:

Ability to work remotely (across time zones) but collaboratively with multiple stakeholders

Understanding of Asian context including regional partnerships

Knowledge of Access to medical products

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Knowledge of standard tools (Word, Excel, PowerPoint, MS Team and Zoom)

Languages and level requiredย Essential:

Expert knowledge of EnglishDesirable: Intermediate or basic knowledge of another UN language

Locationย Off site: home based. The consultant must be available during working hours for South East Asia.ย 

Travelย The consultant will be expected to travel.

Remuneration and budget (travel costs are excluded)

Remuneration:ย Band level B โ€“ USD 7'000 - USD 9'980 per month

Living expenses (A living expense is payable to on-site consultants who are internationally recruited):N/A

Expected duration of contract:ย ย ย 11 months with a possibility of extension subject to availability of funds and satisfactory performance.

Additional Information

This vacancy notice may be used to identify candidates for other similar consultancies at the same level.Only candidates under serious consideration will be contacted.A written test may be used as a form of screening.If your candidature is retained for interview, you will be required to provide, in advance, a scanned copy of the degree(s)/diploma(s)/certificate(s) required for this position. WHO only considers higher educational qualifications obtained from an institution accredited/recognized in the World Higher Education Database (WHED), a list updated by the International Association of Universities (IAU)/United Nations Educational, Scientific and Cultural Organization (UNESCO). The list can be accessed through the link: http://www.whed.net/. Some professional certificates may not appear in the WHED and will require individual review.For information on WHO's operations please visit: http://www.who.int.WHO is committed to workforce diversity.WHO has a smoke-free environment and does not recruit smokers or users of any form of tobacco.Applications from women and from nationals of non and underrepresented Member States are particularly encouraged.WHO prides itself on a workforce that adheres to the highest ethical and professional standards and that is committed to put the WHO Values Charter into practice.WHO has zero tolerance towards sexual exploitation and abuse (SEA), sexual harassment and other types of abusive conduct (i.e., discrimination, abuse of authority and harassment). All members of the WHO workforce have a role to play in promoting a safe and respectful workplace and should report to WHO any actual or suspected cases of SEA, sexual harassment and other types of abusive conduct. To ensure that individuals with a substantiated history of SEA, sexual harassment or other types of abusive conduct are not hired by the Organization, WHO will conduct a background verification of final candidates.Consultants shall perform the work as independent contractors in a personal capacity, and not as a representative of any entity or authority. The execution of the work under a consultant contract does not create an employer/employee relationship between WHO and the Consultant.WHO shall have no responsibility whatsoever for any taxes, duties, social security contributions or other contributions payable by the Consultant. The Consultant shall be solely responsible for withholding and paying any taxes, duties, social security contributions and any other contributions which are applicable to the Consultant in in each location/jurisdiction in which the work hereunder is performed, and the Consultant shall not be entitled to any reimbursement thereof by WHO.Consultants working in Switzerland must register with the applicable Swiss cantonal tax authorities and social security authorities, within the prescribed timeframes (Guidelines issued by the Swiss Mission are available at: https://www.eda.admin.ch/missions/mission-onu-geneve/en/home/manual-regime-privileges-and-immunities/introduction/Manuel-personnes-sans-privileges-et-immunites-carte-H/Non fonctionnaires et stagiaires.html

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