Associate Clinical Safety Professional (temporary position – 12 months)

Location:

Søborg – Denmark

Salary:

Competitive

Type:

Permanent

Main Industry:

Search Health, Nursing & Social Services Jobs

Other Industries & Skills: 

Utilities & Services

Job ID:

132706042

Posted On: 

17 February 2026

Research & Development

Soeborg, Denmark

Do you want to contribute to the safety and quality of Novo Nordisk clinical development products? Would you like to use your medical knowledge to handle serious adverse events reported from clinical trials? Would you thrive in a well-regulated area where you make sure that global regulatory requirements are complied with?   

Then you might be the Associate Clinical Safety Professional we are looking for. Read more and apply today for a life-changing career!

Your new role   

As an Associate Clinical Safety Professional, you will play a key role in handling serious adverse events reported from our clinical trials to ensure that global regulatory requirements are met.

Your main responsibilities will include:

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-Handle serious adverse events in the Veeva safety database and ensure sure that the reports are accurately and consistently registered and evaluated
-Assess the reports including need of requesting missing information on the reported events 
-Take part in the conduct of clinical trials. Here you will maintain overview of individual adverse event reports in a specific clinical trial
-Be responsible for communication to relevant stakeholders regarding specific safety issues and other relevant information
-Cross functional collaboration and internal communication will therefore be a part of your everyday work
-Assist with related administrative and procedural activities and ensure that all tasks are performed in compliance with GxP requirements
 

Your new department  

Safety Operations Case Management Department is part of Safety Operations and one of the operational areas in Global Patient Safety. Global Patient Safety is responsible for meeting global regulatory requirements for handling and reporting of adverse events. We ensure the surveillance of safety and quality of Novo Nordisk clinical development and marketed products. Our department consists of three Case Management teams, each with 14 highly engaged colleagues.  

Skills and qualifications  

We are looking for a candidate who has the following qualifications:

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-B.Sc. degree or M.Sc. degree, registered nurse or equivalent within health science
-Experience working in clinical setting
-Experience with clinical trials or pharmacovigilance (experience within the fields of diabetes, cardiology or obesity is an advantage)
-Experience using Veeva Safety Database or other Veeva modules
-Extensive knowledge of medicinal terminology and clinical pharmacology
-Interest in and flair for using IT-systems and strong skills in MS Office
-Proficiency in both written and spoken English is a requirement, as you will be working with international stakeholders
 

With regards to personal skills, you are known for your good analytical skills and ability to collaborate. You are detail-oriented, diligent and have strong communication skills. In addition, you remain calm and focused even when your work becomes unexpected or has periods of changes. 

Working at Novo Nordisk 

Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with an unconventional spirit, a rare determination, and a constant curiosity. For over 100 years, this unordinary mindset has seen us build a company unlike any other. One where a collective passion for our purpose, mutual respect, and a willingness to go beyond what we know delivers extraordinary results. 

What we offer 

There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.   

More information 

For more information, or Martin Duus Holle at DHOEnovonordisk,  Marie Werngreen at MRWGnovonordisk. or Stine Bastian at SBTInovonordisk.

Deadline  

1 March, 2026 

You do not need to attach a cover letter to your application, but please include a few sentences on your motivation for applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo to your CV. 

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk, we’re not chasing quick fixes – we’re creating lasting change for long-term health. For over 100 years, we’ve been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what’s possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we’re making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.

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