Consultant – Senior Regulatory Reviewer (AVAREF Clinical Trial Pilot)
Closing soon — applications close today
Applications close on 12 Nov 2026. Check the employer's notice for the exact closing time.
About this role
WHO is recruiting a Senior Regulatory Reviewer for its AVAREF Clinical Trial Pilot. Senior medical and pharmaceutical regulatory experts can apply before 12 November 2026.
Role details
The World Health Organization (WHO), through its Regional Office for Africa, is seeking an experienced Senior Regulatory Reviewer for its African Vaccine Regulatory Forum (AVAREF) Clinical Trial Pilot.
This consultancy provides an opportunity for highly experienced medical, biomedical, pharmaceutical and regulatory professionals to contribute to clinical trial regulation, medicines assessment and vaccine safety across Africa.
The position is particularly suitable for senior professionals with extensive experience in national medicines regulatory agencies, clinical trial dossier reviews, pharmaceutical regulation and biomedical research.
Organisation: World Health Organization (WHO), Regional Office for Africa Programme: AVAREF Clinical Trial Pilot Duty station: Congo-Brazzaville Work arrangement: Offsite / home-based Job reference: 2604137 Contract type: External consultancy Contract duration: Two months Remuneration: USD 7,000–9,980 per month Published by employer: 29 October 2026 Application deadline: 12 November 2026
About the opportunity
- The consultancy supports WHO's efforts to strengthen clinical trial regulation and improve access to safe, effective and quality-assured medicines, vaccines and other health technologies in African countries.
- The successful consultant will provide specialist technical expertise in regulatory assessments and clinical trial reviews.
Specialist expertise
- Relevant expertise may include clinical trial dossier assessment, vaccine and pharmaceutical registration, Good Clinical Practice inspections, Good Manufacturing Practice, pharmacovigilance, biostatistics, pharmacology and toxicology, and clinical research and regulatory science.
Language requirements
- Excellent knowledge of English and French is essential. Working knowledge of another language is an advantage.
Remuneration
- WHO advertises remuneration of USD 7,000 to USD 9,980 per month for this consultancy, excluding applicable travel costs.
How to apply
- Apply through the official WHO careers portal using the Apply on employer site button on this page.
- Review the complete terms of reference and ensure that your qualifications and professional experience meet the requirements.
- The application deadline is 12 November 2026. Only candidates under serious consideration will be contacted, and WHO may conduct written assessments as part of the recruitment process.
Recruitment safety notice: Apply only through the official WHO careers website. Do not pay individuals or agencies promising guaranteed WHO employment.
Responsibilities
- Reviewing clinical trial applications and regulatory dossiers.
- Assessing clinical and non-clinical evidence submitted for medicines and vaccine registration.
- Supporting regulatory assessments of vaccines, biotherapeutics and other pharmaceutical products.
- Providing technical expertise in pharmacology, toxicology, microbiology and related disciplines.
- Supporting regulatory reviews in accordance with applicable international standards.
- Contributing to Good Clinical Practice (GCP) and Good Clinical Laboratory Practice (GCLP) assessments.
- Supporting pharmacovigilance and post-marketing surveillance activities.
- Preparing technical assessments and regulatory reports.
- Supporting capacity building and regulatory collaboration across African countries.
Requirements
- A Doctorate in Medicine, Biomedical Sciences or Health Sciences, or an advanced university degree (Master's or higher) in a health-related field.
- Additional advanced qualifications in public health, clinical research, pharmacology, toxicology, microbiology, biostatistics or pharmacovigilance are desirable.
- At least 10 years of experience working in an internationally recognised national regulatory agency.
- At least 10 years of experience in the regulation of medicines, vaccines, biotherapeutics, pharmaceuticals or diagnostics.
- At least 10 years of experience reviewing clinical trial dossiers and medicine registration applications.
- Experience in the regulation of biologics and biosimilars.
- Strong analytical, technical writing and communication skills.
- Experience working with international organisations, government agencies, research institutions or the pharmaceutical industry.
- Excellent knowledge of English and French.