Senior Pharmaco-Epidemiologist

Excelya Group; Saclay; Sur place; EUR 65 000 - 85 000; Plein temps

Résumé du poste

A leading mid-size CRO in Île-de-France seeks an experienced professional to lead pharmacoepidemiology and Real-World Evidence projects. You will ensure scientific quality and regulatory compliance while collaborating with cross-functional teams to enhance patient outcomes. The ideal candidate has strong methodological expertise, experience in RWE, and an advanced degree in a relevant field. Fluency in French and English is required, and you'll thrive in a dynamic environment committed to innovation.

Qualifications

• Proven experience in pharmacoepidemiology and/or real-world evidence generation within the pharmaceutical, biotech, or CRO environment.
• Strong methodological expertise in study design, data analysis, and interpretation of real-world data.
• Fluent in French and in English.

Responsabilités

• Lead and coordinate pharmacoepidemiology and RWE projects to address research questions.
• Ensure scientific quality, regulatory compliance, and timely delivery of methodologies and study outputs.
• Contribute to RWE/PE studies conducted internally or with CROs.
• Provide methodological expertise to ensure robust project outcomes.
• Conduct feasibility studies using primary and/or secondary data sources.

Connaissances

Pharmacoepidemiology

Real-World Evidence (RWE) generation

Study design

Data analysis

Regulatory compliance

Feasibility assessments

Bibliographic research

Data source evaluations

Formation

Advanced degree in Epidemiology, Biostatistics, Public Health, or related Life Sciences field

Description du poste

About the Job

oin Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Medical Affairs. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Responsibilities

• Lead and coordinate pharmacoepidemiology and RWE (Real-World Evidence) projects to address research questions using real‑world data
• Ensure the scientific quality, regulatory compliance, and timely delivery of methodologies and study outputs
• Contribute to RWE/PE studies conducted internally or in collaboration with CROs
• Provide methodological expertise (study design, bias management, limitations assessment) to ensure robust project outcomes
• Conduct feasibility studies using primary and/or secondary data sources, as well as bibliographic research in epidemiology and methodology
• Perform data source mapping activities to support RWE initiatives
• Actively participate in project meetings within the Global RWE department and with internal/external stakeholders
• Contribute to the development and improvement of internal standards and guidance for RWD/RWI/RWE activities
• Collaborate with cross‑functional teams to integrate epidemiological insights into global research strategies

Experience

Proven experience in pharmacoepidemiology and/or real‑world evidence generation within the pharmaceutical, biotech, or CRO environment.

Skills

Strong methodological expertise in study design, data analysis, and interpretation of real‑world data, solid understanding of regulatory requirements and best practices for RWE/PE studies. Experience conducting feasibility assessments, bibliographic research, and data source evaluations.

Education

Advanced degree in Epidemiology, Biostatistics, Public Health, or related Life Sciences field (PhD or Master's with relevant experience preferred).

Languages

Fluent in French and in English.

Why Join Us?

At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.

Here’s what makes us unique.

We are a young, ambitious health company representing 900 Excelyates, driven to become Europe’s leading mid‑size CRO with the best employee experience. Our one‑stop provider service model offering full‑service, functional service provider, and consulting enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient’s journey.

Excelling with care

means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.