Accountable and responsible for execution and delivery of complex & accelerated epidemiology & clinical studies to time , budget and quality as defined in the Development plan and study protocol and in adherence with GCP-ICH, GSK vaccines documents and within regulatory requirement. • Develop and follow the most efficient operating model to manage appropriately the risks linked to studies and has experience and skills to manage all associated requirements – Same for the management and… Show more Accountable and responsible for execution and delivery of complex & accelerated epidemiology & clinical studies to time , budget and quality as defined in the Development plan and study protocol and in adherence with GCP-ICH, GSK vaccines documents and within regulatory requirement. • Develop and follow the most efficient operating model to manage appropriately the risks linked to studies and has experience and skills to manage all associated requirements – Same for the management and oversight of outsourced activities.• Manages study communications, Study Risks assessment and issue escalation within the team. • Ensure all systems are correctly populated and up to date• Develop study plans and forecasts, including detailed study schedule management plan and budget• Mentoring experience of junior profiles (Jr SDL, GSK Future Leader Program candidate & WHO Trainee)• Development of the onboarding program and training material for SDL newcomers.• Active member in different taskforces linked to process improvement and simplification (e.g. Third party oversight, clinical supplies)Working on several projects: Malaria (becoming Mosquirix), HSV (becoming Arexvy) Show less

Responsible for all operational aspects of Immunotherapeutics vaccines clinical trials. Accountable for managing external service providers (Clinical Reseach Organization) as part of the outsourcing strategy, when conducting clinical trials.

Responsible for all aseptic operations within Pilot Plant – R&D including organisation, planning and production of all adjuvant systems and candidate vaccine lots intended for use in toxicology and early phase clinical studies. Leading preparation of the Pilot Plant Business Continuity Plan.Responsible for all Environment Health & Safety (EHS) activities including implementation of a selective sorting process of chemical waste, EHS procedures training and coordination of related-survey… Show more Responsible for all aseptic operations within Pilot Plant – R&D including organisation, planning and production of all adjuvant systems and candidate vaccine lots intended for use in toxicology and early phase clinical studies. Leading preparation of the Pilot Plant Business Continuity Plan.Responsible for all Environment Health & Safety (EHS) activities including implementation of a selective sorting process of chemical waste, EHS procedures training and coordination of related-survey. Managing a team of 4 persons Show less

Responsible for all operational aspects of prophylactic vaccines clinical trials including preparation of protocol, study product documentation for Authorities submission, CRF & logistics aspects.

Conducting initiation, monitoring and closure visits in Belgium for Pharmaceutical clinical studies.