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Real World Evidence - Project Manager

Excelya
CompanyExcelya
CategoryOperations & Admin
LocationDilbeek
RemoteOn-site (inferred)
EmploymentFull-time
LevelManager
SalaryNot stated by the employer
Posted18 Jun 2026
Last verified9 Aug 2026
SourceEmployer ATS (workable)
Applications are handled by the employer, not by us.Apply on the employer's site →
Description
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. 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 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 About You At Excelya, taking audacious steps is encouraged, so we're looking for individuals who are ready to grow with us and share our values. Experience:  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). Skills:  Understanding of how RWE supports pricing, reimbursement, and managed entry agreements, Proven ability to lead complex RWE projects and manage multiple stakeholders. Education:  MSc or higher in a medical or scientific field. Languages:  English mandatory & French and/or Dutch Benefits 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.