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Toxicology Study Monitor

Toxicology Study Monitor

Date: Jul 30, 2019

Location: Braine L'alleud, Walloon Brabant, BE

UCB, Brussels, Belgium (www.ucb.com) is a global biopharmaceutical company focused on the Discovery and development of innovative medicines and solutions to transform the lives of people living with severe diseases of the immune system or of the central nervous system. With more than 8 500 people in about 40 countries, the company generated revenue of € 4.5 billion in 2017. UCB is listed on Euronext Brussels (symbol: UCB)

Within the Non-Clinical Safety Team part of Development Science Function located at its main European production site in Belgium, UCB is looking for a Toxicology Study Monitor

You will be responsible for the thorough management and monitoring of non-clinical safety studies with NCE and NBE therapeutic 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. You will record, escalate, and manage study-related issues, including their resolution together with internal/external subject matter experts. You will 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.

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.

To your internal customers you offer with enthusiasm the expertise in toxicology-related fields which you gained through a solid scientific background, either holding a degree in Biology or Veterinary or being a Pharmacist; with at least 5 years of experience as a Preclinical Study Director/Monitor of in vivo studies (with various species) within a CRO or pharmaceutical industry.

To apply please go to www.ucb.com/careers.

Discover more about the remarkable UCB Talent Blends and how you can contribute to the mix at www.ucb.com/careers.

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Toxicology Study Monitor

UCB, Braine-l'Alleud
Permanent contract
Developer