World Health Organization (WHO) is the directing and coordinating authority for health within the United Nations system. It is responsible for providing leadership on global health matters, shaping the health research agenda, setting norms and standards, articulating evidence-based policy options, providing technical support to countries and monitoring and assessing health trends.
We are recruiting to fill the position below:
Job Title: Roster of Consultants - Clinical Expertise for the assessment of vaccines for the purpose of the WHO Prequalification and Emergency Use Listing
Job ID: 2403984 Location: Anywhere
Expected duration of contract: Contract duration varies based on the programme needs
Contractual Arrangement: External consultant
Organization: HQ/VAX Vaccines & Immunization Devices Assessment
Background
The World Health Organization (WHO), through its Regulation and Prequalification Department provides advice to the United Nations Children’s Fund (UNICEF) and other United Nations agencies on the acceptability, in principle, of vaccines considered for purchase by such agencies. This service is called prequalification.
The purpose of the WHO prequalification assessment is to provide assurance that candidate vaccines: (a) meet WHO recommendations on quality, safety and efficacy, including compliance with WHO’s recommended standards for good manufacturing practices (GMP) and good clinical practice (GCP); and (b) meet the operational packaging and presentation specifications of the relevant United Nations agency. Prequalification also supports the specific needs of national immunization programmes with regards to vaccine characteristic such as potency, thermostability, presentation, labelling and shipping conditions.
The aim is to ensure that vaccines provided through the United Nations for use in national immunization services in different countries are safe, effective and suitable for the target populations at the recommended immunization schedules and with appropriate concomitant products.
This important work is carried out with the support of international experts in Non-Clinical, Clinical and Chemistry, Manufacturing and Controls (CMC) evaluation of biological medicinal products, specifically vaccines. WHO is making a call to increase the number of consultants/experts available to support this very important public health responsibility.
Deliverables
Produce timely assessment reports (AR) of the reviewed information.
Report on critical, major, and other deficiencies detected during the review of the documentation/data (assigned to the consultant).
Assess the applicant's responses to queries raised in the AR and decide on the adequacy of each response. Several sets of queries may be necessary.
Provide WHO with a recommendation and final remarks on the evaluation based on the documentation assigned for review to the consultant. This should be based on the most updated scientific and regulatory grounds.
Qualifications, experience, skills and languages
Educational Qualifications:
Essential:
Advanced university degree in medicine, biology, or pharmacy.
Desirable:
A postgraduate degree in biostatistics or in epidemiology with focus on infectious diseases or related science.
Experience:
Essential:
Over ten years’ experience in the field of infectious diseases, immunization and regulation of biological products including vaccines acquired by working in the field of immunization or community and preventive medicine at country or international level and/or with a National Regulatory Authority (NRAs), with at least 5 years respective experience at the national level.
Extensive experience in the evaluation of clinical trials for vaccines.
Desirable:
Experience at international level.
Work experience in developing countries.
Skills:
Essential:
Solid clinical scientific background, particularly in the area of infectious diseases and vaccines
Expert must have technical skills and knowledge on the development, strengthening and monitoring of regulatory systems for vaccines, drugs, biologicals, and medical devices.
Desirable:
Familiarity with WHO prequalification procedure, with WHO activities in strengthening the capacity to regulate clinical trials, vaccines as a biological medical product and /or with the NRA assessment procedure.