Arbejde Team Leader Hovedstaden Novo Nordisk A/S - jobtilbud
jobbeskrivelse:
- Team Leader - 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. Novo Nordisk Regulatory Affairs is seeking a Team Leader for our team in Søborg, Regulatory Affairs Victoza®. If you thrive in a dynamic and challenging environment with focus on regulatory execution, this job offers you the opportunity to be part of the daily management of regulatory activties for Victoza® for type 2 diabetes. About the department Regulatory Affairs Victoza® works with Victoza® our blockbuster GLP-1 agonist for treatment of type 2 diabetes and with other liraglutide projects for treatment of diabetes. Our responsibilities include outlining the regulatory strategies, interacting with regualtory authorities and managing the regulatory submissions to obtain and maintain marketing authorisations worldwide for Victoza®. We have a project centric organisation and you will work in cross-functional teams. Our key external stakeholders are the regulatory authorities. The job You will be responsible for coordinating, planning, preparing and submitting high quality dossiers to the authorities and to ensure fast approvals for Victoza® in type 2 diabetes. Part of your everyday work will include the daily management of the regulatory team including prioritisation of the use of team resources, coordinate assignments and ensure that targets are met. Furthermore, you will ensure team development and daily people management. We work with several very different submissions, and thus, you need to be able to handle several tasks at the same time. This requires good coordination and planning skills as well as accountability and the ability to work under tight deadlines including high workloads in periods. You will be a key player in keeping track of timelines and deliverables. You will work closely together with the team consisting of regulatory professionals and associates on the regulatory submissions and ensuring approvals. You will report to the director of Regulatory Affairs Victoza® Qualifications You hold a master of science or PhD. You must have experience from regulatory affairs including experience with managing label updates and lifecycle management submissions worldwide. Therapeutic understanding within type 2 diabetes is an advantage. You have a proven record in global regulatory understanding and have extensive working experience within the pharmaceutical industry. You have demonstrated management competencies or have management experience. You are proactive, have a can-do mindset and you are capable of setting directions and following-up on deliverables. Furthermore, you like working in a team, you are flexible, able to work under tight deadlines and have a strong quality mindset. Good coordination and planning skills and an excellent command of written and spoken English is a must. Learn more about us: novonordisk.com/RD-careers Working at Novo Nordisk At Novo Nordisk, we work together to prevent, treat and eventually cure diabetes. Nearly 371 million people worldwide are living with diabetes today, with two people diagnosed with the disease every ten seconds. Working here is not just a way to make a living, but a way to make a difference. Contact for further information, please call Lene Melchiorsen on +45 3075 1993. Deadline 23 December 2014.
Arbejdsgiver Navn: Novo Nordisk A/S
Arbejdsgiver telefonnummer: 44448888
Arbejdsgiver faxnummer: 44442314
Job kort beskrivelse: Farmaceutarbejde
land: Danmark
region: Hovedstaden
Kontrakt varighed: Fast
Kontrakttype: Fuldtid
krævede uddannelse: Ikke angivet
Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark
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