The Nordic Real World organization is a multidisciplinary consulting team serving life science and healthcare stakeholders with insights and advice. In Real World we aim to serve Nordic pharma companies and other stakeholders with Nordic treatment insights based on Real World data and Real World Evidence studies. We actively collaborate with hospitals, regional payers and national registries on research and policy related topics.

As a Junior Analyst focusing on Real World Solutions, you will work on interesting projects for Nordic clients. Analysts will work under direct supervision of a senior colleague, they will assist with the development, review and analysis of study material and as well as in the development of client solutions. As an Analyst you are responsible for delivering work independently with some guidance and should be able to lead smaller projects or defined work streams. Your analytical, inter-personal and project management skills will be called upon from day one.

Every project will be different but an idea of the things that you are expected to accomplish are the following:

• 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.

About you:

Candidates interested in joining as a Real World Analyst should have:

• 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.

Nice To Have:

• Previous experience with Nordic registry data and submitting data access applications.

• Previous experience in statistical programming in secondary database studies.

• Working experience as CRA in the Nordics (or equivalent experience).

• High digital affinity and MS Office (Word, PPT, Excel) skills are an advantage.

• Working experience in oncology and/or neurology.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.