RWE Project Lead: Real World Evidence & Strategy

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

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