Senior Evidence and Outcomes Specialist (Pharmaceutical, Valby)

Job summary

The role involves designing and executing evidence generation studies to enhance product positioning and ensure access, focusing on real-world database analytics and clinical trial analyses.

Qualifications

• Master’s or PhD in Epidemiology, Biostatistics, Health Economics, Data Science, or a related quantitative field.
• At least 7 years of experience in analyzing real-world data and clinical trial data within consulting or the pharma/biotech sector.
• Proficient in working with healthcare databases, including claims, EHR, and registries, with skills in data cleaning and manipulation.
• Knowledge of psychometric analyses for Clinical Outcome Assessment validation.
• Familiarity with regulatory and payer guidance related to real-world data (FDA, EMA, JCA).
• Strong understanding of observational study design and advanced statistical methods.
• Proven track record of scientific publications in peer-reviewed journals.
• Excellent communication skills with the ability to convey complex analyses into actionable insights.
• Solid quantitative and programming skills in tools such as SAS, R, or Python.

Responsibilities

• Conduct real-world database analytics and post hoc analyses of randomized clinical trials.
• Collaborate with cross-functional teams including Medical Affairs, Market Access, and Clinical Development.
• Coordinate projects with sponsors and manage independent work.
• Analyze data to derive insights that meet business evidence strategy needs.

Skills

• Strong analytical and problem-solving skills.
• Ability to work collaboratively in a team-oriented environment.
• Creative and curious mindset with a focus on independent work.

Education

• Advanced degree (Master’s or PhD) in a relevant field.

Tools

• Proficiency in statistical programming languages such as SAS, R, or Python.