Preclinical Study Director Permanent £67,000 – £80,000 As a Preclinical Study Director, you will be responsible for overseeing the planning, execution, and reporting of preclinical studies in compliance with regulatory standards (e.g., GLP). You will lead and coordinate cross-functional teams, ensuring the scientific rigor and integrity of studies aimed at evaluating the safety, pharmacology, and toxicology of novel drug candidates. This role requires strong project management skills, a deep understanding of experimental design, and the ability to communicate complex data to both scientific and non-scientific audiences. Develop and design preclinical studies (e.g., toxicology, pharmacokinetics, efficacy) in collaboration with scientific teams and regulatory departments Ensure that study protocols are aligned with company goals and comply with GLP and regulatory requirements Serve as the main point of contact and scientific lead for preclinical studies, ensuring smooth coordination with internal teams and external CROs Manage study timelines, budgets, and resources, ensuring that studies are completed on time and within budget Oversee the collection, analysis, and interpretation of preclinical data, ensuring the scientific quality and integrity of results Prepare and review comprehensive study reports, ensuring accuracy, completeness, and adherence to regulatory requirements Lead cross-functional project teams, including toxicologists, pharmacologists, lab technicians, and external collaborators Act as a liaison between the preclinical research team and other departments such as clinical development, regulatory affairs, and quality assurance Ensure all studies are conducted in compliance with Good Laboratory Practice (GLP) regulations and other relevant regulatory guidelines What we’re looking for: PhD in Pharmacology,, Biology, or related scientific field (Master’s degree with significant relevant experience may be considered) Minimum of 4 years of experience in preclinical research within the pharmaceutical or biotechnology industry Experience in designing, executing, and interpreting preclinical toxicology or pharmacology studies Strong scientific knowledge in pharmacology, toxicology, or related disciplines Excellent project management skills with the ability to manage multiple studies simultaneously This position is ideal for a driven and scientifically motivated individual seeking to make a significant impact in the development of novel therapies through preclinical research