Study Director – Toxicology

Position: Study Director – Toxicology

Role Overview:

The Study Director – Toxicology will be responsible for designing, conducting, overseeing, and reporting non-clinical safety studies (GLP and non-GLP) to support drug development and regulatory submissions. The role involves scientific leadership, regulatory compliance, study management, and cross-functional collaboration to ensure the quality and integrity of toxicology studies.

Key Skills & Experience

• Experience in repeat-dose toxicity, teratology, and reproductive toxicity studies/processes.
• Understanding of pharmaceutical R&D and agrochemical testing processes.
• Strong knowledge of GLP and relevant regulatory guidelines.
• Proven experience as a Study Director or in an equivalent role within a CRO or pharmaceutical organization.
• Strong scientific writing and communication skills.
• Ability to lead teams and manage multiple projects simultaneously.
• Proficiency in data analysis and scientific interpretation.
• Strong team-working and cross-functional collaboration skills.

Behavioral Competencies

• Excellent oral and written communication skills.
• Flexibility to work effectively in a dynamic environment.
• Effective time and project management skills.
• Takes ownership of responsibilities and demonstrates a commitment to continuous learning and improvement.
• Well-organized, structured, and efficient approach to work.

• Qualification: Ph.D./Master's in Veterinary Sciences, Biosciences, or related disciplines.