Senior Pharmaco-Epidemiologist at Excelya

Saclay, Ile-de-France, France -

Full Time

Start Date

Immediate

Expiry Date

30 Mar, 26

Salary

0.0

Posted On

30 Dec, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Pharmacoepidemiology, Real-World Evidence, Study Design, Data Analysis, Bias Management, Limitations Assessment, Feasibility Studies, Bibliographic Research, Data Source Mapping, Regulatory Compliance, Methodological Expertise, Collaboration, Cross-Functional Teams, Internal Standards, Guidance Development

Industry

Pharmaceutical Manufacturing

Description

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. 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 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.

Responsibilities

Lead and coordinate pharmacoepidemiology and RWE projects to address research questions using real-world data. Ensure scientific quality and regulatory compliance while contributing to internal and collaborative studies.