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reference: 4872589

documentId: 4872589

connectionPointId: 7

lastModificationDate: 1535978372800

stillingsbetegnelse:
Safety Surveillance Principal Specialist in Cardiology, Global Safety

jobbeskrivelse:

Do you want to play a key role in ensuring highest safety and lowest possible risk to patients that use Novo Nordisk products? And would you like to be part of one of the most skilled and advanced safety functions in Denmark? You may be our new colleague in Safety Surveillance.

About the department
Safety Surveillance is a department within Global Safety and is situated in Bagsværd, Denmark. Our team of dedicated and skilled professionals has global responsibility for the surveillance of all safety information for Novo Nordisk’s products that are currently marketed or under development.

The position
You will deliver clinical, medical and scientific expertise in relation to important cardiological safety issues identified across the Safety Surveillance function.

Additionally, you will be supporting the ongoing safety surveillance of one or more key products in early phase clinical development. This responsibility includes critical analysis and medical evaluation of the emerging aggregate safety data and establishment of the product safety profile during development. You will also be involved in preparing communications about the benefit risk assessment and you may be our safety representative in cross-functional teams.

Furthermore, you will contribute to development of clinical trial protocols and clinical trial reports where you will provide medical/clinical input. Your job responsibilities also include chairing one or more cross-functional drug safety committees and communication with external parties related to clinical safety monitoring such as Data Monitoring Committees.

You will get the opportunity both to work independently and in collaboration with a team of highly skilled, committed and enthusiastic colleagues. Assuming responsibility, communicating information 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, Non-Clinical Development and the Regulatory Affairs team and it will give you an extensive insight to the whole Novo Nordisk organisation.

Qualifications
You are a MD with a proven clinical and scientific background (doctoral thesis, PhD, or publications) in cardiology.

You probably also have prior experience within pharmacovigilance from the pharmaceutical industry or you have experience from clinical development within the pharmaceutical industry and strong urge to specialise within pharmacovigilance.

As a person you are ethical, responsible, well-organised and a strong communicator. You are able to work under pressure when needed. You are a strong collaborator and a dedicated team player who thrives in a multicultural environment of continuous development and you are good at establishing contact and collaborating with stakeholders.

You are fluent in English both written and spoken (company language) and an experienced user of MS Office.

Working at Novo Nordisk
At Novo Nordisk your skills, commitment and ambition help us change lives for diabetes and obesity patients 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 contact Poul-Martin Haahr at +45 3075 4082.

Deadline
24 September 2018.

numberOfPosts: 1

jobCategoriesCodes_0: http://data.europa.eu/esco/isco/C2211

abstractJV_contact_0:
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positionTypeCode: directhire

contractTypeCodes_0: fulltime

Arbejdsgiver Navn: NOVO NORDISK A/S

source: DK-STAR