Toxicology Study Monitor, Braine-l'Alleud

il y a 3 semaines

Brainel'Alleud, Wallonie, Belgique TN Belgium Temps plein

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Client:

UCB

Location:

Braine-l'Alleud, Belgium

Job Category:

Other

EU work permit required:

Yes

Job Reference:

72da113733f7

Job Views:

24

Posted:

23.01.2025

Expiry Date:

09.03.2025

Job Description:

Make your mark for patients

We are looking for a Toxicology Study Monitor to join us in our Non-Clinical Safety Evaluation organization based in Braine-l'Alleud, Belgium.

About the role:

The position is based in the UCB laboratories and offices at the Braine-l'Alleud campus.

What you will do:

  • 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.

Who you will work with:

  • You will work with both internal and external stakeholders.

Interested? For this position you'll need the following education, experience and skills:

  • You are autonomous and efficient, you excel at communicating technically and graphically.
  • You are 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 apply:

We 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-renowned 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.

Internal 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.

Please note that if you are NOT a passport holder of the country for the vacancy you might need a work permit. Check our Blog for more information.

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