About this role
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. 📩 Interested candidates may send their CV to:
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