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7 Dec 2020

Full-Time Preclinical Study Monitor (Tox & DMPK)

UCB Bioscience – Posted by UCBdenise Boston, Massachusetts, United States

Job Description

At UCB, we put our heart, soul and skills into making a difference for people living with significant unmet needs. Working together, we blend the best of our talents to deliver thoughtful solutions that patients value. Will you join us in this pioneering adventure?





We are currently seeking a Preclinical Study Monitor (Tox & DMPK). As preclinical Study Monitor, you will be responsible for the thorough management and monitoring of non-clinical safety and DMPK studies.



You like to work in an environment where you can:


  • Use your influencing skills to monitor the CRO and to ensure the on-time release of pivotal final reports
  • analyze, interpret, contextualize and present final reports
  • work on Different therapeutic areas and modalities: NCE, NBE, peptides, new modalities like gene therapy and potential studies to explore new formulations for Zilucoplan extended release.


You will contribute by:


  • designing, initiating, 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.
  • recording, escalating, and managing study-related issues, including their resolution together with internal/external subject matter experts


Minimum Qualifications


  • BSc, ideally MSc in toxicology or related fields
  • Autonomous and efficient, the candidate needs to excel at communicating technically and graphically.
  • Organized and systematic, a proactive team player who is used to work in international matrix environments.
  • To internal customers the candidate will offer with enthusiasm the expertise in toxicology/DPMK-related fields gained through a solid scientific background and several years (min 4 years) of experience as a Preclinical Study Director/Monitor of in vivo studies (with various species) within a CRO or pharmaceutical industry.


Preferred Qualifications


  • Prior experience with TPD or gene therapy is a plus
  • Relevant CRO experience
  • DABT/ERT certification
  • PhD in Toxicology or related field is a plus



About Us

At UCB, we come together every day to work, laser-focused, on a simple question: How will this create value for people living with severe diseases? By putting patients at the heart of everything we do, our approach – from discovery to development to delivery – is continuously transformed and designed around patient needs and their journey.

With a team of approximately 7,500 employees worldwide operations in more than 40 countries, we are a global biopharmaceutical company investing more than a quarter of our revenue in cutting-edge scientific research. We are focused on addressing chronic, neurological, immunological, and bone diseases. We are looking for people with passion and empathy who develop a real understanding of patient’s needs and can deliver thoughtful solutions to decisionmakers across the heath care ecosystem.

Curious to know more? Please visit our website

How to Apply

Job Categories: Equal Opportunities. Job Types: Full-Time. Salaries: Not Disclosed.

Job expires in 41 days.

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