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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.

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* 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

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* 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:

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* 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