GlaxoSmithKline Biologicals (GSK Biologicals), la division vaccins du groupe GSK, se définit comme une entreprise mondiale de recherche, de développement et de production de vaccins à la pointe de l’innovation dans la lutte contre les infections et les maladies les plus menaçantes. La Belgique est le quartier général mondial de la division vaccins qui emploie plus de 11000 personnes dans le monde, dont quelques 8000 sont répartis entre trois sites belges : Rixensart, Wavre et Gembloux. Le réseau global de GSK Biologicals, comptant 15 sites de production stratégiquement positionnés à travers le monde, est consacré à la recherche et au développement clinique, aux activités de production, ainsi qu’au contrôle et à l’assurance qualité.

The same Immunotherapy approach is also valid for the treatment of other disease like Alzheimer or Smoking Addiction, and this is also part of the program pursued by GSKBIO. For its Antigen-Specific Cancer Immunotherapeutic(s) - ASCI(s) we are looking for a (m/f):



You are working within the Clinical Development Management team. Your main responsibility is to support the Clinical Development Manager in effective implementation of the clinical development plan.
As Clinical Scientist, you’ll be working close collaboration with the clinical operations department who’ll handle the operational aspect of the clinical studies whereas you will act as the scientific reference towards the GSK local teams, Study Centres and external partners. This implies the following:
- you coordinate the implementation of regional/global studies;
- you monitor the clinical projects in terms of milestones and bridge the timing and feasibility information from Clinical Operations to the Clinical Development Manager;
- you visit the GSK local operating companies and possibly selected study sites to discuss the projects and help in sustaining recruitment
- you collaborate, within ASCI Business Unit, to dedicated project planning and tracking across clinical functions (Biostat, Scientific Writing, Data Management, Clinical Development Management, Global Study Manager/Leader)
- you prepare and follow-up IDMCs (Independent Data Monitoring Committees), trial steering committees and advisory committees and interacts with study sites, ethics committees, competent authorities as needed
- you contribute to the development of briefing documents, regulatory files, protocols and end of study reports together with the Scientific Writing and the Clinical Development Manager.


- you hold a PhD in Life Sciences or a PharmD;
- you have experience in clinical research at an international level in Oncology or in CNS
- you have an excellent understanding of Clinical Study Management activities and have occupied a function in Clinical Study Conduct in the pharmaceutical industry for at least 5 years;
- you are English fluent, any other language is an asset.
- you consider travelling up to 30% of the time


- A challenging job within a highly innovative GSK Bio programme;
- A contribution to high-tech research and development in the field of cancer
- A growing, confident and ambitious business to be a part of driven by science, performance and the pride to ensure a healthier an happier life to patients