20 beste vacatures voor de functie van clinical project in zaventem, vlg (nieuwe medewerkers gezocht)

Senior Real World Evidence Expert (Belgium)
UCB —Anderlecht
- Doctoraat
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Senior Analyst, Product Management – PD Life Cycle Management
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- Marketing
- Engels
- Microsoft Office
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Medicine Specialist (Fluent in French) - Freelance AI Trainer Project
Meridial —Brussel
- € 8 - € 65 per uur
- Thuiswerk
- Geneeskunde
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Medpace, Inc. —Leuven
- Voltijds
- Engels
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- Bachelor
Senior/ Medical Writer - FSP (M/W/D)
IQVIA —Zaventem
- Voltijds
- Microsoft Word
- Doctoraat
- Onderzoek
Regulatory Submission Lead
GlaxoSmithKline —Waver
- € 57.900 - € 96.500 per jaar
- Voltijds
- Bachelor
- Agile
- Artificiële intelligentie
9 dagen
Doctoral Candidate position HORIZON-MSCA-DoctoralNetwork SPACE-MEL 3D multiomics
KU Leuven —Leuven
- € 3.120,64 per maand
- Voltijds
- Doctoraat
- Engels
- Onderzoek
Medical Monitor (Gastroenterology)
PSI CRO —Leuven
- Voltijds
- Hybride werken
- Geneeskunde
- Doctoraat
- Onderzoek
Snel solliciteren
Performance Analyst - V.I.E Programme
Eurofins Campus —Brussel
- Voltijds
- Microsoft Excel
- Microsoft Office
- Financiën
Snel solliciteren
Business Systems and Validation Analyst III
Thermo Fisher Scientific —Zaventem
- Voltijds
- Thuiswerk
- Microsoft Office
- Analytisch vermogen
- Bachelor
R&D and PV Compliance Lead
UCB —Eigenbrakel
- Onderzoek
- Master
- Bachelor
Project Manager (Real Estate)
Eurofins —Brussel
- Voltijds
- Microsoft Powerpoint
- Microsoft Excel
- Master
Snel solliciteren
Medical staff member head & neck radiology – radiology department
UZ Leuven —Leuven
- Deeltijds
- Doctoraat
Senior Clinical Research Associate - Sponsor dedicated - Belgium - Home based (m/w/d)
IQVIA —Zaventem
- Voltijds
- Thuiswerk
- Onderzoek
- Master
- Managementervaring
VIE Bioanalytical Scientist
UCB —Eigenbrakel
- Bachelor
Strategic Project Manager
Corilus —Machelen
- Hybride werken
- PMP
- ERP systemen
- Master
(Senior) Manager Logistics Consulting – Life Science
Bluecrux —Mechelen
- Voltijds
- Hybride werken
- ERP systemen
- Master
Snel solliciteren
Clinical Trial Supply Manager – Brussels, Belgium (F/M)
Sotec Consulting —Brussel
- Voltijds
- Master
- Managementervaring
- Communicatieve vaardigheden
Manager, Product Management – Peritoneal Dialysis Life Cycle Management
Vantive —Eigenbrakel
- Marketing
- Engels
- Microsoft Office
7 dagen
Senior Quality Engineer - Qualified Person
Labcorp —Mechelen
- Voltijds
- Engels
- Onderzoek
- Master

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Senior Real World Evidence Expert (Belgium)

UCB -
Anderlecht

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Vacaturegegevens

Vaste Jobs

Kwalificaties

Doctoraat
Master
Gegevensverzameling
Communicatieve vaardigheden

Volledige vacaturetekst

Make your mark for patients

We are looking for a Senior Real World Evidence Expert who is scientifically rigorous, strategically minded, and passionate about generating impactful real‑world evidence to help shape key decisions across the lifecycle of UCB’s assets, based in Slough, UK or Brussels, Belgium

About the Role

As a Senior RWE Expert, you will autonomously design, lead, and deliver a wide range of global real‑world evidence (RWE) studies. Your work will inform internal decision-making, support regulatory and payer interactions, and contribute to the scientific understanding of disease areas. In addition to overseeing project delivery, you will help shape asset‑level RWE strategies and propose innovative approaches to evidence generation in partnership with the RWE Strategy Lead.

Who You’ll Work With

You will collaborate with statistical teams, RWE Analysts, epidemiologists, clinical teams, Evidence Synthesis partners (HE/HTA), Safety/Pharmacovigilance, external vendors, medical experts, and cross‑functional asset teams. You will serve as an influential scientific contributor with the ability to engage diverse stakeholders and ensure RWE outputs meet strategic, regulatory, and scientific needs.

What You’ll Do

Lead execution of complex global RWE studies using diverse methodologies and datasets end‑to‑end.
Develop study concepts, write protocols, shape analysis plans, and ensure governance and QC compliance.
Deliver epidemiology, natural‑history, burden‑of‑disease, safety‑outcome, regulatory, and comparative‑effectiveness studies.
Represent RWE on primary data‑collection teams and lead high‑visibility secondary data‑use initiatives.
Collaborate with vendors, clinicians, statisticians, and analytics teams to deliver scientifically robust outputs.
Interpret results and communicate findings internally and externally across scientific and strategic forums.
Co‑define evidence needs with HE/HTA partners, Safety, and other functions to support regulatory and payer interactions.
Contribute to asset‑level RWE strategy and propose innovative study designs, data sources, and analytic approaches.
Advocate for rigorous scientific methodology and challenge assumptions using strong methodological reasoning.
Help advance RWE functional excellence through thought leadership, innovation, and best‑practice sharing.

Interested? For this role we’re looking for:

Master’s degree, PhD, or MD in a life science, epidemiology, outcomes research, HEOR, statistics, or related field.
Experience designing and delivering RWE studies using primary or secondary data in pharma, academia, or consultancies.
Strong quantitative and methodological expertise across epidemiology, pharmacoepidemiology, and outcomes research.
Ability to develop high‑quality scientific communications (abstracts, manuscripts, posters, presentations).
Excellent communication skills with the ability to influence and engage cross‑functional and senior stakeholders.
Proven ability to lead projects independently, think strategically, innovate, and adapt in fast‑changing environments.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.

Why work with us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.

At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on [email protected]. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

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clinical project vacatures in zaventem, vlg

Senior Real World Evidence Expert (Belgium)

Senior Analyst, Product Management – PD Life Cycle Management

Medicine Specialist (Fluent in French) - Freelance AI Trainer Project

Contractspecialist Klinisch Onderzoek

Senior/ Medical Writer - FSP (M/W/D)

Regulatory Submission Lead

Doctoral Candidate position HORIZON-MSCA-DoctoralNetwork SPACE-MEL 3D multiomics

Medical Monitor (Gastroenterology)

Performance Analyst - V.I.E Programme

Business Systems and Validation Analyst III

R&D and PV Compliance Lead

Project Manager (Real Estate)

Medical staff member head & neck radiology – radiology department

Senior Clinical Research Associate - Sponsor dedicated - Belgium - Home based (m/w/d)

VIE Bioanalytical Scientist

Strategic Project Manager

(Senior) Manager Logistics Consulting – Life Science

Clinical Trial Supply Manager – Brussels, Belgium (F/M)

Manager, Product Management – Peritoneal Dialysis Life Cycle Management

Senior Quality Engineer - Qualified Person

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van clinical project in zaventem, vlg

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