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.
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.

PhD (or equivalent) in pharmacology/ bio-medicine/ epidemiology or other relevant scientific subject.
Around 3 years of relevant working experience.
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.

Consultant – Real World Solutions, Healthcare & Life Sciences

Key skills