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 workplace. 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.
Qualifications
Qualification: Ph.D./Master's in Veterinary Sciences, Biosciences, or related disciplines.
Additional Information
Interested candidates may send their CV to:
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📌 Study Director – Toxicology (Bengaluru)
🏢 Eurofins
📍 Bengaluru
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