Chef de Projet Rwe H/F Excelya
- Paris - 75
- CDI
- Bac +5
- Industrie Pharmaceutique • Biotechn. • Chimie
Les missions du poste
JoinExcelya,whereAudacity,Care,andEnergydefinewhoweareandhowwework.Webelieveincreatingboldsolutionsandfosteringaninclusiveenvironmentwherecollaborationandindividualgrowthgohandinhand.
Thisroleisanexcitingopportunitytocontributetoadynamic,ambitiousteam.Youwillplayacriticalpartindrivinginnovationandmakinganimpactintheclinicalresearchspace,whileenjoyingastimulatingprofessionalenvironmentthatencouragespersonalandintellectualgrowth.
Main responsibilities:
- Lead multiple Real World Evidence (RWE) studies and projects from inception to completion, ensuring timelines and budgets are met.
- Oversee study design and execution, including protocol review and operational planning.
- Manage vendors such as CROs and data providers, ensuring quality and compliance.
- Utilize primary and secondary real-world data sources for evidence generation.
- Integrate digital tools and platforms for data collection and analysis.
- Collaborate cross-functionally with internal teams (Medical Affairs, Market Access) and external stakeholders.
- Prepare and deliver progress reports and updates to senior management.
- Align RWE strategies with market access objectives, including pricing and reimbursement considerations.
- Identify opportunities to innovate and integrate RWE into broader business strategies.
Le profil recherché
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'sleading mid-size CROwith thebest employee experience. Ourone-stop provider service modeloffering 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 caremeans 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.
- Expertise in leveraging real-world data and digital tools for evidence generation, Knowledge of the French healthcare and market access landscape, Strong understanding of RWE methodologies (observational studies, registries, pragmatic trials, chart reviews, post-authorization safety studies).
- Understanding of how RWE supports pricing, reimbursement, and managed entry agreements, Proven ability to lead complex RWE projects and manage multiple stakeholders.
- MSc or higher in a medical or scientific field.
- English & French
Bienvenue chez Excelya
Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of full-service CRO, FSP, and Resourcing solutions guided by our values Energy, Care and Audacity.
Founded in 2014 and headquartered in Paris, France, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas.
We take a one-team approach to work: our shared success is the result of collaboration at every stage of a project, from regulatory affairs and clinical operations to quality assurance and strategic development.
Excelya is committed to helping our clients deliver life-changing therapies collaboratively, so we can transform tomorrow together.
Publiée le 12/09/2026 - Réf : edb659f0-bfad-4883-b7d7-e4b984865076
