Site source : Talent BE Lieu : Machelen Flanders Société : Oxford Global Resources Détail de l'offre : including but not limited to basic regulatoryaffairs activities such as QRD-template leaflets,..a pharmaceutical company based in Belgium is looking for a (Junior) RegulatoryAffairsSpecialist a to come on board and join their team...
Site source : Talent BE Lieu : Machelen Flanders Société : Oxford Global Resources Détail de l'offre : The successful candidate will be responsible for managing regulatoryaffairs activities related to clinical trials,..
Site source : Talent BE Lieu : Machelen Flanders Société : Oxford Global Resources Détail de l'offre : Requirements:Life Sciences background.Basic regulatoryaffairs knowledge and experience within the pharmaceutical or biotechnology industry.Fluent in English,..
Site source : Talent BE Lieu : Machelen Flanders Société : Oxford Global Resources Détail de l'offre : The successful candidate will be responsible for managing regulatoryaffairs activities related to clinical trials,..
Site source : Talent BE Lieu : Machelen Flanders Société : Oxford Global Resources Détail de l'offre : a pharmaceutical company based in Belgium is looking for a (Junior) RegulatoryAffairsSpecialist a to come on board and join their team...
Site source : Talent BE Lieu : Machelen Flanders Société : Oxford Global Resources Détail de l'offre : Requirements:Life Sciences background.Basic regulatoryaffairs knowledge and experience within the pharmaceutical or biotechnology industry.Fluent in English,..
Site source : Talent BE Lieu : Machelen Flanders Société : Oxford Global Resources Détail de l'offre : Requirements:Life Sciences background.Basic regulatoryaffairs knowledge and experience within the pharmaceutical or biotechnology industry.Fluent in English,..
Site source : Talent BE Lieu : Machelen Flanders Société : Oxford Global Resources Détail de l'offre : Prepare and maintain QRD-template leaflets in accordance with regulatory requirements.Ensure compliance with Belgian packaging requirements for clinical trial products.Demonstrate experience with type IA & IB variations and other regulatory submissions.Process administrative ..
