WHO Senior Regulatory Reviewer Consultant Job 2026 – Home-Based Opportunity Paying Up to $9,980 Monthly
The World Health Organization (WHO) is inviting applications for an experienced Consultant – Senior Regulatory Reviewer (AVAREF Clinical Trial Pilot) to support the strengthening of clinical trial regulatory systems across Africa.
This consultancy offers an opportunity for highly experienced regulatory scientists, medical professionals and clinical trial reviewers to contribute to an important continental initiative aimed at improving the quality, efficiency and coordination of clinical trial reviews.
The successful consultant will provide technical expertise, mentorship and coaching to regulatory reviewers from 16 African countries participating in the African Vaccine Regulatory Forum (AVAREF) Clinical Trial Pilot Project.
The position is home-based, with the primary location listed as Congo-Brazzaville. The consultancy runs for two months and offers remuneration ranging from USD 7,000 to USD 9,980 per month.
Interested candidates must submit their applications before 13 November 2026.
WHO Senior Regulatory Reviewer Consultant Job Overview
- Organisation: World Health Organization (WHO)
- Position: Consultant – Senior Regulatory Reviewer
- Programme: AVAREF Clinical Trial Pilot
- Job Reference: 2604137
- Location: Home-Based
- Primary Location: Congo-Brazzaville
- Contract Type: External Consultancy
- Contract Duration: Two months
- Work Schedule: Full-time
- Monthly Remuneration: USD 7,000–9,980
- Application Deadline: 13 November 2026
- Required Languages: English and French
About the World Health Organization
The World Health Organization is the United Nations specialised agency responsible for international public health. It works with governments and partners to strengthen health systems, improve access to essential healthcare and address global health challenges.
Through its regional programmes, WHO supports African countries in improving regulatory capacity, strengthening public health institutions and expanding access to safe, effective and quality-assured medicines and vaccines.
The Senior Regulatory Reviewer consultancy forms part of WHO’s work through AVAREF to strengthen clinical trial oversight and improve regulatory collaboration across Africa.
About the AVAREF Clinical Trial Pilot Project
The African Vaccine Regulatory Forum (AVAREF) is a network of National Regulatory Authorities (NRAs) and National Ethics Committees (NECs), established by WHO to strengthen regulatory and ethical oversight of clinical trials.
The Clinical Trial Pilot Project was initiated following an AVAREF Advisory Committee meeting in Dakar in September 2024.
The initiative involves 16 African member countries that nominated 48 expert reviewers across clinical, non-clinical and quality assessment areas.
The project aims to improve cooperation between African regulatory authorities, reduce delays in clinical trial approvals and strengthen the quality and consistency of regulatory decisions.
It also supports the development of harmonised standard operating procedures, digital submission platforms and coordinated review processes.
The consultant will help develop the technical capacity of participating reviewers and support the implementation of joint clinical trial assessments.
Key Responsibilities
The Senior Regulatory Reviewer will work closely with the AVAREF Secretariat Coordinator, participating member states and the 48 nominated reviewers.
Main responsibilities include:
1. Training, Coaching and Mentorship
- Provide technical training to reviewers participating in the Clinical Trial Pilot.
- Mentor and coach clinical reviewers in evaluating clinical trial applications.
- Strengthen reviewers’ ability to assess clinical components of regulatory dossiers.
- Support continuous professional development.
2. Regulatory Guidelines and Procedures
- Assist in updating clinical trial review guidelines.
- Develop and improve standard operating procedures.
- Prepare checklists and technical tools for evaluating clinical trial applications.
- Support harmonisation and standardisation of regulatory review processes.
3. Multi-Country Joint Reviews
- Provide expert support during multi-country clinical trial reviews.
- Participate in scientific advice activities.
- Support facilitated registrations of clinical trials and emergency use authorisations.
- Provide technical guidance to participating regulatory authorities.
4. Training Workshops and Capacity Development
- Develop and deliver training workshops.
- Facilitate comprehensive clinical trial application review training.
- Train reviewers in preparing and writing assessment reports.
- Support the wider capacity-strengthening objectives of AVAREF.
Expected Deliverables
The consultant will be expected to produce the following outputs:
- A report documenting coaching and mentorship provided to reviewers participating in the AVAREF Clinical Trial Pilot.
- A report covering participation in multi-country joint reviews, scientific advice and facilitated registrations.
- Facilitation and delivery of AVAREF workshops as required.
Education Requirements
Applicants must possess one of the following essential qualifications:
- Doctorate in Medicine, Biomedical Sciences or Health Sciences; OR
- An advanced university degree (master’s degree or higher) in a health-related field, such as medicine or health.
Additional qualifications in public health, communicable and non-communicable diseases, pharmacology, toxicology, microbiology, biostatistics, pharmacovigilance or pharmacoepidemiology are desirable.
Specialist clinical qualifications in areas such as cardiology, oncology, paediatrics, internal medicine, infectious diseases and other relevant medical disciplines are also considered valuable.
Professional Experience Requirements
This is a highly specialised consultancy intended for senior regulatory professionals.
Candidates must demonstrate:
- At least 10 years of experience working in an internationally recognised national regulatory agency with WHO Maturity Level 4 (ML-4).
- At least 10 years of experience in medicines regulation, including vaccines, biotherapeutics, pharmaceuticals, advanced therapeutics and diagnostics.
- At least 10 years of experience reviewing clinical trial dossiers and registering new or existing medicines.
- At least 10 years of experience in regulating biotherapeutics, biosimilars and other biological products.
Applicants should also demonstrate expertise in clinical and non-clinical data assessment, Good Clinical Practice inspections, Good Manufacturing Practice, pharmacovigilance, biostatistics or pharmacoepidemiology.
Experience working in Africa, other low- and middle-income countries and advanced economies is desirable.
Strong analytical, scientific writing, communication and teamwork skills are also required.
Language Requirements
Excellent knowledge of English and French is required. Working knowledge of the other language will be an advantage.
Salary and Contract Benefits
The consultancy offers remuneration under Band Level B, ranging from USD 7,000 to USD 9,980 per month.
The initial contract duration is two months. The consultant will work as an independent contractor and will be responsible for applicable taxes, social security contributions and other statutory obligations.
How to Apply for the WHO Senior Regulatory Reviewer Consultant Job
Interested and qualified candidates should submit their applications through the official WHO recruitment platform.
Applicants should ensure that their educational qualifications and professional experience clearly demonstrate the specialised regulatory expertise required for this consultancy.
Application Deadline: 13 November 2026.
Important Information for Applicants
WHO may use a written test as part of the selection process. Candidates shortlisted for an interview may be required to provide scanned copies of their academic degrees, diplomas and professional certificates.
WHO particularly encourages applications from women and nationals of non- and underrepresented Member States.
The organisation does not charge application or recruitment fees at any stage of its selection process.
This consultancy is particularly suited to senior regulatory scientists with substantial experience in clinical trial evaluation, medicines regulation and strengthening national regulatory systems.
