Chef de Projet RWE

Excelya; Paris; Sur place; EUR 90 000 - 130 000; Plein temps

Résumé du poste

Excelya in Paris is seeking a senior Real World Evidence expert to lead multiple RWE studies from design through execution. You will collaborate with Medical Affairs, Market Access, and external stakeholders to deliver timely evidence, optimize study plans, and manage CROs ensuring high-quality data.

English and French required for international collaborations. Join a dynamic team focused on innovative healthcare solutions, with opportunities to influence pricing, reimbursement strategies, and

Qualifications

• Expertise in leveraging real-world data for evidence generation.
• Knowledge of the Belgian healthcare and market access landscape.
• Strong understanding of RWE methodologies (observational studies, registries, pragmatic trials).
• English & French language proficiency.

Responsabilités

• Lead multiple Real World Evidence (RWE) studies from inception to completion, ensuring timelines and budgets.
• 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.

Connaissances

RWE methodologies

Data analysis

English

French

Formation

MSc or higher in medical/scientific field

Outils

Digital data tools

Description du poste

JoinExcelya,whereAudacity,Care,andEnergydefinewhoweareandhowwework.Webelieveincreatingboldsolutionsandfosteringaninclusiveenvironmentwherecollaborationandindividualgrowthgohandinhand.

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

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

Requirements

• Expertise in leveraging real-world data and digital tools for evidence generation, Knowledge of the Belgian 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

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'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.