Excelya

Real World Evidence - Project Manager

Excelya  •  Dilbeek, BE (Onsite)  •  15 days ago
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Job 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.

Excelya

About 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 compassion, care, and excellence. 

Founded in 2014 and headquartered in Paris, France, and operating in 28 countries across Europe, USA and India, 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, with speciality focus on Oncology & Hematology, Rare Disease & Pediatrics, Infectious Disease, Inflammation & Immunotherapy, Pain Treatment & CNS, and Late Phase & RWE.

Industry
Chemicals & Materials
Company Size
501-1,000 employees
Headquarters
Boulogne-Billancourt, FR
Year Founded
2014
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