Designing, conducting, overseeing, and reporting non-clinical safety studies (GLP and non-GLP)
Providing scientific leadership and ensuring regulatory compliance
Managing studies and leading teams
Cross-functional collaboration

🎯 Requirements

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 equivalent in a CRO or pharmaceutical organization
Strong scientific writing and communication skills
Ability to lead teams and manage multiple projects

🛃 Visa sponsorship

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