Project Manager Pre-Clinical Research / Toxicology (m/f/d)

As the experts in digestive and metabolic medicine and as a family-owned business with a global presence, we focus on developing and marketing innovative medicines to treat a wide range of gastrointestinal disorders like inflammatory bowel disease or eosinophilic esophagitis as well as hepatobiliary disorders such as primary biliary cholangitis. Our aim: to meaningfully improve therapeutic practice as well as patient health and well-being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for:

• #### Your tasks
• In this scientifically oriented position, you will be responsible for the oversight, and evaluation of preclinical and toxicological studies. You will contribute to the translational development of drug candidates and ensure the scientific and regulatory integrity of all preclinical data packages.
• Key Responsibilities
• Scientific oversight and coordination of preclinical and toxicology studies conducted in collaboration with CROs, academic partners, and scientific institutions - covering both GLP-regulated and exploratory/non‑GLP research
• Comprehensive data interpretation, including assessment of pharmacological and toxicological endpoints, integration of findings across studies, and development of scientifically substantiated conclusions
• Evaluation of study reports and scientific summaries, ensuring accuracy, transparency, and regulatory compliance
• Compilation of preclinical and toxicology data for regulatory filings, in collaboration with internal and external experts
• Preparation of scientific and toxicological expert assessments, in cooperation with relevant subject-matter experts as needed
• Systematic literature research and integration of external evidence into internal development strategies

• #### Your qualification
• Completed degree in medicine, life sciences, pharmacy, toxicology, veterinary medicine, or a closely related field
• Several years of industry experience in pharmacological or toxicological research (ideally in drug development)
• In‑depth understanding of regulatory requirements for preclinical studies (e.g., GLP, ICH, OECD guidelines)
• Strong analytical and conceptual thinking, with a high level of scientific accuracy
• Ability to manage complex, multidisciplinary projects and work effectively with internal and external scientific stakeholders
• Proficiency in standard MS Office applications.
• Team player with strong motivation and inter-personal skills
• Fluent in English (written and spoken) and ideally also in German