Arbejde Manager of Safety Surveillance Biopharm unspecified NOVO NORDISK A/S - jobtilbud

GÆLDER
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reference: 4910581

documentId: 4910581

connectionPointId: 7

lastModificationDate: 1543321273940

stillingsbetegnelse: Manager of Safety Surveillance Biopharm

jobbeskrivelse:

Do you want to play a key role in the further development and drive the ongoing safety surveillance activities of products in Biopharm portfolio? And would you like to be part of one of the most skilled and advance safety functions in Denmark? Are setting direction and inspiring a team of highly engaged professionals your key competencies? Then you may be the new manager for the Biopharm team.

 

About the department

Safety Surveillance Biopharm Diabetes, Insulin & Devices is a department within Global Safety and is situated in Bagsværd, Denmark. We have global responsibility for the surveillance of all safety information for Novo Nordisk’s products that are currently marketed or under development in Biopharm, Insulins and Devices portfolio. Within the Safety Surveillance Biopharm Diabetes, Insulin & Devices department, we have the Biopharm team dedicated to handle all safety surveillance activities for our Biopharm products pertaining to growth deficiency and bleeding disorders etc.

 

The position

You will be responsible for leading a team consisting of 6-10 drug safety/ pharmacovigilance experts while ensuring the safety strategy and execution of plans, including safety signal detection and risk management activities pertaining to Biopharm products.

 

You will work in a fast-paced environment reflecting the increasing demands from regulatory authorities while always bearing the patient in mind. It will be your job to set direction for your team and to contribute to quality improvement projects.

 

Your job responsibilities will also include supervising the internal Novo Nordisk safety committees within the relevant therapeutic areas.

 

Assuming responsibility, cross-functional collaboration, international communication and taking action will be essential parts of your work day. You will have a close collaboration and interaction with other functional areas in Novo Nordisk, especially the Clinical Development team and Regulatory Affairs team.

 

Qualifications

Preferably you are a Medical Graduate (MD). Alternatively you may have a university degree within Natural Sciences (DVM, MSc. Pharm. or equivalent). You have a minimum 5 years of experience from the pharmaceutical industry in the medical/clinical development or drug safety departments. A solid understanding of medical concepts, disease processes, scientific methodology, drug development and data analysis is very important, documented scientific training (e.g. PhD) and experience from interactions with regulatory authorities will be an additional advantage.

 

You will also preferably have successful experience with people management.

 

You have high personal integrity and are responsible, well-organised, a strong communicator, able to work under pressure when needed and able to make independent decisions regarding drug safety issues.

 

You are a strong driver and a dedicated team player, who thrives in a global environment of continuous development and you are good at establishing contact and collaborating with stakeholders at all levels.

 

You must be fluent in English (both written and spoken) and be an experienced user of MS Office (Excel, PowerPoint, Word and Outlook).

 

Working at Novo Nordisk

At Novo Nordisk, your skills, commitment and ambition help us change lives for diabetes patients for the better. In exchange, we offer you a chance to work with extraordinary talent and to develop both professionally and personally.

 

Contact

For further information, please contact Wasim Anwar at +45 3079 6766.

 

Deadline

30 November 2018.

 

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.
 



numberOfPosts: 1

jobCategoriesCodes_0: http://data.europa.eu/esco/isco/C1349

abstractJV_contact_0: Please apply using one of the specified channels

positionTypeCode: directhire

contractTypeCodes_0: fulltime

Arbejdsgiver Navn: NOVO NORDISK A/S

source: DK-STAR

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