Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Sr. Real World Evidence Analyst (EU)

Job

Datavant

Remote

Full-Time

Posted 6 weeks ago (Updated 2 days ago) • Actively hiring

Expires 8/4/2026

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
51
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Sr. Real World Evidence Analyst (EU) 6727 Barcelona, Spain Full-time regular Now Datavant is the data collaboration platform trusted for healthcare. Guided by our mission to make the world's health data secure, accessible and actionable, we provide critical data solutions for organizations across the healthcare ecosystem - including providers, health plans, researchers, and life sciences companies. From fulfilling a single patient's request for their medical records to powering the AI revolution in healthcare, Datavanters are building the future of how data is connected and used to improve health. By joining Datavant today, you're stepping onto a driven and highly collaborative team that is passionate about creating transformative change in healthcare.
DESCRIPTION
As a science-driven healthcare analytics company with a rapidly growing customer base, Datavant is seeking a Senior Real-World Evidence Analyst with experience analyzing healthcare data. As a Senior Real-World Evidence Analyst in the Research+Analytics (R+A) team, your main role will be to plan, execute, and communicate analyses using real-world data (RWD). You will be part of a team of epidemiologists, biostatisticians, and analysts that contributes to the delivery of scientific projects for our clients.
RESPONSIBILITIES
Study Design & Protocol Development Aid in the scientific feasibility of observational studies Aid in the development of observational study protocols and statistical analysis plans (SAP), which may include tasks such as literature reviews or code lists development Study Implementation & Data Analysis Develop a deep understanding of our internal analytic products (RWE Generation application) Lead and support the implementation of real-world evidence studies which may include: Translating the study protocol into study implementation and results Working with real-world healthcare data, including claims database and electronic healthcare records, to define and build measures for analysis execution. Executing data analysis using internal products (RWE Generation application) or tools such as R or SQL Delivering study results, including the preparation and communication of results tables, figures etc. Develop and maintain knowledge on real-word data sources Customer Support May be asked to work with customers to guide them in designing, creating and delivering scientific results using our RWE Generation application. Collaboration Collaborate closely within the R+A team and partner closely with leads on the Scientific Consulting team. Collaborate with cross-functional teams such as the Product Management and Engineering teams to contribute to the development of analytic product features.
QUALIFICATIONS
Required Qualifications Bachelor's degree (or equivalent), preferably in sciences, social sciences, or a related analytic field with at least 2 years of full-time experience in a research or analytic area OR Master's degree in Public Health, Epidemiology, or Biostatistics Demonstrated experience in analytical research using healthcare data, preferably healthcare claims and/or electronic health records (EHR) data. Outstanding attention to detail and organization. Strong ability for critical and logical thinking Strong ability to quickly learn new tools. Strong ability to self-motivate and manage conflicting priorities in a fast-paced environment. Excellent communication in verbal and written form. Preferred Qualifications Experience with analytic or statistical software programs (e.g., R, SAS). Experience with epidemiological studies or familiarity with epidemiology concepts. Perks of joining Datavant in Barcelona 25 vacation days Daily in-office lunch stipend (and a fully stocked kitchen) Hybrid work model: 2 days/ week in our office in Gracia Commitment to professional development opportunities Employee-led initiatives including annual company-wide innovation day & DEI resource groups Comprehensive private health coverage w/ out-of-network reimbursements options Flexible remuneration with Cobee (Restaurant, Transportation, Nursery) Peer & company recognition programs Monthly educational lunch & learns To ensure the safety of patients and staff, many of our clients require post-offer health screenings and proof and/or completion of various vaccinations such as the flu shot, Tdap, COVID-19, etc. Any requests to be exempted from these requirements will be reviewed by Datavant Human Resources and determined on a case-by-case basis. Depending on the state in which you will be working, exemptions may be available on the basis of disability, medical contraindications to the vaccine or any of its components, pregnancy or pregnancy-related medical conditions, and/or religion. This job is not eligible for employment sponsorship.