Study Director – Toxicology and In Vivo Pharmacology

An established scientific research organization is seeking an experienced Study Director in Toxicology and/or In Vivo Pharmacology to lead and oversee non-clinical studies supporting pharmaceutical, biotechnology, chemical, and related life science programs.

The Role

As a scientific project manager, you will be responsible for the design, execution, interpretation, and reporting of non-clinical toxicology and pharmacology studies. Working closely with multidisciplinary teams, you will ensure studies are conducted in accordance with client requirements, applicable quality standards, and internal procedures.

Key responsibilities include:

• Managing GLP and non-GLP in vivo toxicology and pharmacology studies in rodent and non-rodent species.
• Developing study protocols and experimental designs.
• Coordinating study execution and supervising cross-functional project teams.
• Collecting, analysing, and interpreting scientific data.
• Preparing high-quality scientific reports and study documentation.
• Ensuring compliance with established quality systems, procedures, and regulatory requirements.
• Collaborating with support functions including Quality Assurance and Documentation teams.
• Acting as a scientific subject matter expert and contributing to the continuous improvement of departmental capabilities, methodologies, and technical expertise.
• Supporting client interactions through the presentation and discussion of study results.

What you’ll need:

• A minimum of 10 years' experience managing experimental life science studies within research, pharmaceutical, biotechnology, chemical, or related organizations.
• Strong technical expertise in toxicology, pharmacology, pharmacokinetics, or a closely related discipline.
• Knowledge of immunology, which would be considered an advantage.
• Experience interacting with internal and external stakeholders, including presenting scientific findings and discussing study outcomes.
• Proven experience working within highly regulated quality environments (e.g., GLP, ISO, or equivalent standards).
• Excellent scientific writing, analytical, and project management skills.
• PhD in Toxicology, Pharmacology, or a related discipline

Languages

• Fluent English (minimum C1 level) with excellent written and verbal communication skills.
• Ability to communicate effectively with international clients and colleagues.