Toxicology Study Monitor

☞ UCB

Vue: 130

Jour de mise à jour: 03-12-2025

Localisation: Braine-l’Alleud Walloon Brabant

Catégorie: Autre

Industrie: Pharmaceutical Manufacturing

Niveau: Entry level

Type d’emploi: Full-time

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le contenu du travail

Make your mark for patientsTo strengthen our Non-Clinical Safety Evaluation team, we are looking for a high caliber, self-motivated, Toxicology Study Monitor based in Braine l’Alleud, BelgiumAt UCB everything we do starts with a simple question: “How will this make a difference to the lives of people living with severe diseases?” We do that by connecting our ground-breaking science with patients and their families around the world living with the physical and social burdens of autoimmune and neurological disorders. Those connections offer new perspectives, drive innovation, and offer the hope of a new generation of therapies that will help improve lives on a global scale. You like to work in an environment where you will:
  • Be responsible for the thorough management and monitoring of non-clinical safety studies with NCE, NBE and Gene Therapy modalities: design, initiation, scheduling, protocol development, interactions with Test Facilities and Test Sites, coordination of study material shipments, compliance with UCB policies, quality, regulatory, animal welfare and in-house SOP, tracking phases and contributor reports.
  • Record, escalate, and manage study-related issues, including their resolution together with internal/external subject matter experts.
  • Monitor the study progress with the CRO, circulate relevant documents to all contributing scientists, analyze, interpret, contextualize and present the results and ensure the on-time release of the pivotal final report.
Interested? For this position you’ll need the following education, experience and skills:
  • Autonomous and efficient, you excel at communicating technically and graphically.
  • Organized and systematic, you are a proactive team player used to work in international matrix environments
  • To your internal customers you offer with enthusiasm the expertise in toxicology-related fields which you gained through a solid scientific background and several years of experience as a Preclinical Study Director/Monitor of in vivo studies (with various species) within a CRO or pharmaceutical industry.
Why you should applyWe can offer you an informal and open working environment that does not lock scientists into structure and hierarchy.  Freedom to take space to pursue your own ideas and make a difference.  Opportunity to gain internal and external visibility through interactions with other UCB teams and with world-renown academic investigators. Opportunity to grow both as a drug hunter and leader through participation in project teams and our career/personal development programs.At UCB, we strive to attract passionate and outstanding talents who thrive on change and are ready to bring real value to patients. Working for us you’ll discover a place where you can grow and express your full potential. We place an emphasis on innovation, collaboration and impact. Through meaningful recognition and a motivating work atmosphere, we aim to provide an optimal experience by caring about and valuing our employees – just as we do for the patients we serve.If you believe you are the perfect match to join us on our pioneering adventure, then we invite you to apply and tell us more about your profile and motivation.If you want to learn more about R&D within UCB go to R&D at UCB .RANDATUCBInternal applicants should be in their current job for at least 12 months, must meet performance standards and are not on formal corrective/disciplinary process (PIP), warning, final warning, or compliance warning letters within the last 12 months. Please inform your Manager or your Talent Partner before applying to any internal job opportunities.UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity.Requisition ID: 85296Recruiter: Romina RosettiHiring Manager: Marie-Luce RosseelsTalent Partner: Geraldine Beauduin
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Date limite: 17-01-2026

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