Scientist Preclinical Development, Safety and Toxicology (m/f/x)

We are looking for a scientist who will help us to drive our preclinical projects. You would be working in a team with experienced scientist and support our Chief Scientific Officer. 

In particular, you would 

  • Act as study monitor and manage multiple IND-enabling preclinical studies (GLP / non-GLP compliant, single and multi-site) performed at external contract research organizations (CROs) 
  • Coordinate, plan, and monitor preclinical safety and tolerability studies for all development programs  
  • Assist study protocol development, review study results, reports, regulatory files, and any other study-related documentation  
  • Support qualification and selection of preclinical CROs and maintain regular interaction with CROs to ensure quality, proper information flow and contract performance 
  • Manage study operations logistics (e.g., compound delivery to sites, multi-site shipment of samples) 
  • Be responsible for scientific communications (internally and with CROs) 

Here is how to convince us:  

  • You have a scientific background in toxicology, biology, chemistry, pharmacy, veterinary medicine, or other relevant scientific discipline (at least Master’s degree). 
  • A minimum of 2 years of experience in the design and execution of preclinical studies in a pharmaceutical industry company or Preclinical Research Organization 
  • In-depth understanding of toxicology and working knowledge with animal models is a plus (handling, drug administration, anesthesia, organ harvest, tissue histology and quantitative microscopy, etc.) 
  • Sound knowledge of GLP principles and international drug development guidance (EMA, FDA, ICH). 
  • Project management experience with focus on early-stage drug development  
  • Excellent interpersonal skills and ability to work in a team environment 
  • Very good written and oral communication skills in English language (German is a plus) 

What we offer: 

  • A full-time position (or part time, minimum 30 hours)  
  • A fair salary commensurate with your experience 
  • You can participate in the success of our company 
  • A highly innovative and motivated team where you can rely on your colleagues 
  • Cross-functional work experience withing an international team and flat hierarchies 

Please send your meaningful application specifying your salary expectations as well as the earliest possible starting date by email to  

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