Conduct thorough qualitative and quantitative research (for both scientific and non-scientific focused projects)
Reach out and liaise with potential sites (e.g. hospitals, data holders) and stakeholders such as KOLs, Payers, Clients etc; for set up of contracts, project meetings, confidentiality agreements and applications
May serve as project manager on small-sized client engagements
May perform CRA Site Management visits
Write and/or review data access applications to Nordic health data authorities (e.g. patient-level data, aggregate data requests)
Conduct interviews with local clinical experts as well as with patients
Create well-structured, client-facing deliverables and communicate insights
Stay up to date on the national health data landscape in your country
May contribute to proposal development

MSc or PHD (or equivalent) in pharmacology/ bio-medicine/ epidemiology or other relevant scientific subjects
Experienced and comfortable with basic statistics (e.g. mean, median, percentiles, p-values, confidence intervals, survival analysis)
Proven project management skills and willingness to broaden experience
Excellent communication skills in English and at least one Nordic language, living in the Nordics
Good and comfortable at structuring information in a logical way
Excellent interpersonal skills and ability to work effectively with others across the Nordic countries and with global excellence centres
Adaptability and an ability to learn quickly and apply new knowledge

Analyst, Real World Solutions, Healthcare & Life Sciences

Key skills