Senior Pharmaco-Epidemiologist

Excelya; Saclay; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading mid-size CRO is seeking a professional to lead pharmacoepidemiology and real-world evidence projects. You will be responsible for ensuring methodological quality and regulatory compliance, conducting feasibility studies, and collaborating with cross-functional teams. The ideal candidate should have substantial experience in pharmacoepidemiology and an advanced degree in a relevant field. Additionally, fluency in both French and English is required for effective communication in a dynamic environment driven by innovation and collaboration.

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 using real-world data.
• Ensure scientific quality and regulatory compliance of study outputs.
• Conduct feasibility studies and provide methodological expertise.

Connaissances

Pharmacoepidemiology

Real-World Evidence generation

Study design

Data analysis

Feasibility assessments

Formation

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

Description du poste

About the Job

Join 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.

Main 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

Requirements

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.

Benefits

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.