stillingsbetegnelse: Regulatory Professional

jobbeskrivelse:
- Regulatory Affairs - Denmark - Søborg Our growth is your opportunity Being part of Novo Nordisk Research & Development means working at one of the world's largest and most successful biopharmaceutical companies. Our R&D organisation is vital to Novo Nordisk's continued growth and we always welcome talented people who would like to grow with us. Join a fast-changing environment where engaged people do their best every day to get Novo Nordisk medicines approved across the globe. Our people have a unique combination of scientific insight and the ability to navigate many agendas and stakeholders. That makes Regulatory Affairs a truly interesting place to work but also challenging. Are you up for the challenge? About the department RA Biopharm- hGH is part of Regulatory Affairs. In our area we are a dedicated and diverse team of 30 people located in Søborg, Denmark. As a team, we are breaking new ground within the therapeutic areas of growth hormone and hemophilia. Furthermore we are supporting all marketed products with growth hormone, Hemophilia and hormone replacements. In this dynamic environment, our dedicated group prepares the regulatory strategies and is responsible for global interactions with regulatory authorities. We work closely with many different stakeholders within Novo Nordisk headquarters and affiliates. We have a strong team-spirit and together we go the extra mile to succeed. The Job The position which is a 1 year temporary position is situated in Søborg. You will be part of a team consisting of a Project Manager as well as experienced Regulatory Professionals and Associates. Your role will be to diligently secure the clinical input to global regulatory strategies and submissions. You will plan, coordinate and review regulatory documentation and support internal working groups as our primary sparring partner for the clinical units in Novo Nordisk. To this end, you will work closely with the Regulatory Project Manager who is overall responsible for the regulatory part of our projects. In addition, you will be part of cross functional teams sharing your knowledge and getting new ideas. You will report to the department director. Qualifications As a minimum, we expect you to have a biology/health science university degree. It is an advantage to have some experience from pharmaceutical development working with regulatory aspects of clinical and/or non-clinical development. You work successfully in project teams respecting the contribution of everyone. You demonstrate that you are organised, detail-oriented and a proactive problem-solver. You communicate well and are completely comfortable speaking and writing English and can deal with the challenges of international communication. On a personal level, you thrive in busy and changing circumstances and bring a can-do attitude and a healthy sense of humour. You keep focus on jointly moving the projects and are able to work independently, be challenged and find new solutions. At Novo Nordisk, your skills, commitment and ambition help us change lives for the better. In exchange, we offer you a chance to work with extraordinary talent and to develop professionally and personally. Contact For further information, please call Eva Gamwell Henriksen on +45 3079 6202. Deadline 14 December 2014.

Arbejdsgiver Navn: Novo Nordisk A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse:
Arbejde inden for biologi, botanik, zoologi og beslægtede områder

land: Danmark

region: Hovedstaden

Kontrakt varighed: Fast

Kontrakttype: Fuldtid

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark