Regulatory Affairs Manager till expansivt CRO

TFS AB is working with both international and national projects within many therapeutic fields.The Regulatory Affairs department is involved in a lot of exciting projects in various phases, such as registration strategy planning in early development phase, clinical trial application and marketing approval, as well as maintenance after approval.On a contract basis we also have assignments with consultants outsourced to the clients' sites. The main responsibilities of the Regulatory Affairs Manager will include: .Preparation, review and compilation of regulatory submissions .Liaison with authorities .Advice/answers to regulatory issues/questions .Participate in tasks related to internal regulatory support within TFS .Participate in project work and marketing activities..Maintain a high level of competence regarding international We are looking forward to receiving your application with included CV and a personal letter.