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stillingsbetegnelse:
Safety Surveillance Specialist, Obesity & NASH, 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 diabetes products? And would you like to be part of one of the most skilled and advanced pharmacovigilance 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 surveillance of all safety information for Novo Nordisk’s products that are currently marketed or under development.

 

The position

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, 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 may also include chairing a cross-functional drug safety committee 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 Non-clinical and Clinical Development team and Regulatory Affairs team and it will give you an extensive insight to the whole Novo Nordisk organisation.

 

Qualifications

You have a degree in Natural Science preferably complemented by a PhD or are a Medical Doctor. You probably have prior experience within pharmacovigilance from the pharmaceutical industry or you have experience from early clinical development within the pharmaceutical industry and strong urge to specialise within pharmacovigilance. On top of that, you also have a solid understanding of medical concepts, disease processes, scientific methodology, drug development and documented scientific training.

 

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 30754082.

 

Deadline

28 February 2019.

 

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/C3322

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