Rare Disease - experienced Safety Surveillance Advisers

Fuldtid

Permanent

Gladsaxe

ID: 2564619

Indrykket for 45 dage siden

Do you want to lead and drive safety surveillance activities in development projects in rare diseases? And would you like to be part of one of the most skilled and advanced pharmacovigilance functions in Denmark?

We are expanding and therefore have open positions for experienced candidates in the Safety Surveillance Rare Disease team at Novo Nordisk.

Apply today for a life-changing career!

About the Teams
Safety Surveillance Rare Disease is a team within Global Safety at Novo Nordisk. Our dedicated and skilled professionals have global responsibility for the establishment of the product safety profile during clinical development, and for performing critical analysis and medical evaluation of the emerging aggregate safety data. Due to an increase in the number of development projects, our team is expanding.

In the Rare Disease team, we handle projects within the rare disease indication from development to post marketing. You will in collaboration with other colleagues in the team, be responsible for surveillance activities related to the compounds in development for rare blood and bleeding disease indications.

The Position
Responsibilities may include:

Chair cross-functional drug safety committees.

Prepare communication about the benefit risk assessment.

Contribute to development of clinical study designs and protocols.

Communicate with external parties related to clinical safety monitoring such as Data Monitoring Committees.

Represent Safety Surveillance in cross-functional teams.

You will get the opportunity both to work independently and in collaboration with a team of highly skilled, committed, and enthusiastic colleagues across the functional areas in Novo Nordisk, especially the Non-clinical and Clinical Development teams. Assuming responsibility, communicating information and taking action will be essential parts of your workday.

Qualifications
As an ideal candidate, you will have:

A Master’s degree within Medicine or Natural Sciences (MD, DVM, MSc Pharm or equivalent), possibly complemented by a PhD/research experience

Preferably several years of experience within pharmacovigilance, or within the pharmaceutical industry and a strong desire to specialise within safety surveillance

Interest/experience in data analysis and analysis tools (e.g.Jmp and/or Qliksense)

A solid understanding of medical concepts, scientific methodology, and drug development

Curiosity to explore new ways of analysing data (e.g. could be in the form of optimizing current ways of working)

The ability to work independently as well as to collaborate in a continuous developing environment

It is important that you are a strong collaborator who thrives in a multicultural environment of continuous development, and that you are good at establishing contacts and collaborating with stakeholders out in the organisation as well as external stakeholder’s.

As a person, you are self-driven and able to work independently and under pressure when needed. You are ethical, responsible, well-organised and a strong communicator.

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