Epidemiology Specialist

at  Novo Nordisk

Måløv, Region Hovedstaden, Denmark -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate11 Nov, 2024Not Specified12 Aug, 2024N/AStakeholder Management,Life Sciences,Pharmaceutical Industry,Epidemiology,It,Communication Skills,Project Teams,Pharmacoepidemiology,Cardiovascular Disease,Biostatistics,Public Health,DiabetesNoNo
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Description:

Epidemiology Specialist
Category: Data & AI
Location:Måløv, Capital Region of Denmark, DK
Are you looking for a unique opportunity to impact drug discovery with your epidemiological skills? Would you like to work in a highly scientific, professional, and global environment? Are you ready to join a team of research data scientists and epidemiologists using advanced analytics to improve people’s lives?
Then this may be your opportunity to pursue an exciting career in a global organisation! The department of Computational Precision Health is being established to support decision-making and drug discovery in Research & Early Development. We are looking for a highly motivated, skilled and independent epidemiologist to take the lead on studies and insights using multimodal Real-World Data.
This position is available in Måløv/Hellerup (Denmark) or London (UK).

QUALIFICATIONS

To thrive and succeed in this role, we would expect you to have:

  • A MD, DVM, or Master’s degree in epidemiology, public health, life sciences, biostatistics, or equivalent. A PhD degree in a relevant field would be advantageous
  • Prior significant work experience within pharmacoepidemiology from the pharmaceutical industry or consulting. Experience working on Preclinical projects in the pharmaceutical industry would be advantageous
  • Solid hands-on experience with analytical epidemiological projects and real-world data. Prior experience in chronic diseases such as diabetes, obesity, cardiovascular disease or kidney disease would be advantageous
  • Strong experience in project management and cross-functional stakeholder management

We expect you to be ambitious and innovative. It is essential that you can use your good interpersonal and communication skills to achieve results together with others, both internally and when working with external project teams. You must thrive in a role where you have responsibility, you are proactive and work independently. The job is globally oriented and excellent communication skills together with interest in co-operating with stakeholders across the globe is essential.

Responsibilities:

Your main responsibilities will be to:

  • Identify impactful real-world evidence needs by proactively liaising with a broad range of stakeholders across R&ED
  • Provide epidemiological evidence and expertise to stakeholders internally and externally
  • Conduct varied and diverse tasks within pharmaco- and classical epidemiology, including taking the lead on guiding study designs and analytical methods
  • Identify and determine efficient data collection approaches and data sources
  • Design analyses that will be conducted in collaboration with data scientists based on the data from external collaborations, Novo Nordisk observational studies, or from external commercial data sources
  • Perform and guide epidemiological synopsis or study protocol creation
  • Participate in cross-functional working groups as the lead subject matter expert on pharmacoepidemiology topics
  • Communicate your results and findings in a clear and convincing way both orally and in reports, and peer reviewed scientific paper

To thrive and succeed in this role, we would expect you to have:

  • A MD, DVM, or Master’s degree in epidemiology, public health, life sciences, biostatistics, or equivalent. A PhD degree in a relevant field would be advantageous
  • Prior significant work experience within pharmacoepidemiology from the pharmaceutical industry or consulting. Experience working on Preclinical projects in the pharmaceutical industry would be advantageous
  • Solid hands-on experience with analytical epidemiological projects and real-world data. Prior experience in chronic diseases such as diabetes, obesity, cardiovascular disease or kidney disease would be advantageous
  • Strong experience in project management and cross-functional stakeholder managemen


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Clinical Pharmacy

Graduate

Relevant Field

Proficient

1

Måløv, Denmark