Jobbet "Student Assistant, Safety Surveillance" er udløbet.
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The position
The position is framed for an average of 16 hours/week. During the first 6 months, you should be available to work on either Wednesdays and/or Fridays as one of your working days, to allow adequate overlap with other students, and for training purposes.

As a student assistant in Safety Surveillance, you will be part of part of a dynamic and well-functioning student team of 4 who are responsible for supporting the collection and preparation of regulatory documentation to regulatory authorities around the world. You will be involved in multiple steps and stakeholders across the pharmacovigilance process, i.e., from data retrieval and analysis, drafting of initial reports, to quality control and publishing of the final reports. Your tasks will be a mixture of recurrent and ad hoc tasks, including:

  • Retrieving and preparing data for aggregate safety reports and recurrent signal detection
  • Preliminary data analysis and drafting textual observations and conclusions
  • Frontloading preparation of aggregate safety reports for submission to authorities
  • Contributing to and ensuring timely completion of planned routine surveillance tasks
  • Indexing and processing documents in a document management database
  • Ad hoc tasks.

You will be working with a variety of different tools for creating and managing documents, as well as visual analytics tools.

Requirements for this position are that you: -

  • Are on your 1st or 2nd year of pharmaceutical sciences or equivalent
  • Are structured, reliable and good at time management
  • Have excellent English skills, especially written
  • Have proficient IT skills and a good understanding of Word and Excel.

It is advantageous that you are:

  • Flexible and able to handle multiple tasks at once
  • Detail orientated
  • Able to work well in a team and independently.

About the department
Safety Surveillance is part of the Novo Nordisk Pharmacovigilance area and is responsible for continuously monitoring developing and marketed products to ensure safety and efficacy for patients. The main role of Safety Surveillance is to detect and manage safety signals based on drug side-effects reported spontaneously or collected in clinical trials, perform periodic benefit-risk evaluation, and prepare periodic aggregate safety reports. The department comprises apxm. 80 colleagues of 18 different nationalities.

Working at Novo Nordisk
In Novo Nordisk it is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you:

  • A great, multi-national working environment with open and friendly colleagues
  • A steep but rewarding learning curve where you will gain relevant clinical pharmacovigilance experience
  • Varying and challenging tasks
  • Flexible work hours.

For further information, please contact:  Mark White on 30796710.

30 January 2022.

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

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