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.