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

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 toxic endpoints, integration of findings across studies, and development of scientifically substantiated conclusions Evaluation of study reports and scientific summaryes, accuracy 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 stakeholders Proficiency in standard MS Office applications. Team player with strong motivation and interpersonal skills Fluent in English (written and spoken) and ideally in German

Your benefits Supportive, respectful and appreciative work atmosphere in a small, dedicated team Diverse learning culture and individual development opportunities International and growing family business with short decision-making processes, financial independence and long-term perspective New work, flexible working hours and mobile working Wide range of benefits (free beverages, health and sports benefits, canteen, JobRad) Comprehensive onboarding and mentoring program If you have any questions, please do not hesitate to contact Sabine Aicher at personal@drfalkpharma.de or call 0761 1514-253. We look forward to receiving your application via our online portal.