stillingsbetegnelse: Regulatory Associates

jobbeskrivelse:
- Administrative - Denmark - Søborg Would you like to be part of Novo Nordisk Regulatory Affairs and part of “can-do” department located in Søborg, Denmark? If yes, then we are seeking a Regulatory Associate for the Saxenda product. About the department Regulatory Affairs is an area within Global Research and Development, responsible for obtaining and maintaining marketing authorisations worldwide. This includes interaction with Health Authorities in connection with planning of meetings, submission of clinical trial applications, submission and maintenance of marketing authorisation applications. You will work together with a highly skilled and motivated team responsible for ensuring new marketing authorisation of Saxenda around the world and maintaining already obtained approvals. The job We are looking for a person who enjoys structure, promptness and a dynamic environment. We offer an opportunity to work and grow within an exiting regulatory area. You will collaborate with colleagues from Novo Nordisk in Denmark as well as with affiliates. Part of your everyday work will include a close cooperation with the Regulatory Project Manager on the management of the Global Regulatory Team, quality check of documents for regulatory submissions, and compiling and archiving of electronic documents into our global document management system. Administrative duties and IT systems support will be part of your everyday task. We work with very different submissions and thus you need to be able to joggle several tasks at the same time. You will have close contact with our colleagues’ in other countries as well as work closely with many different departments within Novo Nordisk in Denmark. The job requires working independently and good coordination and planning skills, accountability and the ability to work under tight deadlines including high work loads in periods. You will be a key player in keeping track of timelines and deliverables. You will also be responsible for keeping up to date with current requirements within area of responsibility. Qualifications You have a relevant educational background, as minimum a bachelor’s degree in science, business administration or English. You should have administrative experience from regulatory affairs or related fields in the pharmaceutical industry. You have experience with professional use of IT systems such as electronic document management and are proficient in the Microsoft Office package. You are proactive and like to work independently, as well as in a team. You are flexible, are able to work under tight deadlines, have a strong quality mindset and a sense for details, good coordination and planning skills and an excellent command of written and spoken English. At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development. Contact For further information, please contact Christina Balslev Rindshøj on +45 3075 9092. Deadline 4 December 2015.

Arbejdsgiver Navn: Novo Nordisk A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse: Arbejde inden for samfundsøkonomi

land: Danmark

region: Hovedstaden

Kontrakt varighed: Fast

Kontrakttype: Fuldtid

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark