Arbejde Regulatory Affairs Associate Hovedstaden Novo Nordisk A/S - jobtilbud

GÆLDER
stillingsbetegnelse: Regulatory Affairs Associate

jobbeskrivelse:
- Administrative - Denmark - Søborg Join Regulatory Affairs (RA) and become part of a fast-changing environment where engaged people do their best every day to get Novo Nordisk’s medicines approved across the globe. Our people have a unique combination of scientific insight, patient focus, and the ability to navigate many agendas and stakeholders. That makes Regulatory Affairs a truly interesting place to work – but also quite challenging. We are currently looking for a Regulatory Associate, with an interest in working with Life Cycle Management (LCM) activities, to join the RA Haemophilia department. About the department In the RA Biopharm area we are responsible for all the regulatory activities with clinical and/or labelling impact for Haemophilia, Growth Hormone and Hormone Replacement Therapy (HRT). In RA haemophilia we have three marketed products, NovoSeven®, NovoEight® and NovoThirteen®. We are organised in smaller product teams within the department, however we work in a flexible manner according to work load in the different teams. You will work in a fast paced environment with tight deadlines, and you will be supported by friendly colleagues with a good sense of humour. The job Your primary task will be to handle the administrative tasks needed for clinical LCM of our marketed haemophilia products. You will work closely with the Regulatory Professional and Project Manager, internal stakeholders and affiliates worldwide. You will be responsible for preparing, compiling and submitting documentation to health authorities. You will also handle various requests from affiliates and other stakeholders. Qualifications Preferably, you have experience with working in Regulatory Affairs. You have an educational background as a medical secretary, bachelor in science, marketing, English or similar. You have a flair for IT systems and experience with MS Office applications as you will be responsible for managing data entry and electronic filing in our various databases and document management systems. Fluency in written and spoken English is a must. On a personal level, you are very structured, systematic and you have a strong quality mind-set. You are a team player, but also enjoy working independently. You have a positive attitude, good sense of humour, and you keep your spirits high also under pressure. At Novo Nordisk, we use our skills, dedication and ambition to help people with diabetes. We offer the chance to be part of a truly global work place, where passion and engagement are met with opportunities for professional and personal development. Contact For further information please contact Alice Troy on +45 3075 4026. Deadline 30 September 2015.

Arbejdsgiver Navn: Novo Nordisk A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse:
Operatørarbejde ved fremstilling af kemiske produkter

land: Danmark

region: Hovedstaden

Kontrakt varighed: Fast

Kontrakttype: Fuldtid

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark

GÆLDER

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