Study Director – Toxicology
Core
Designing, conducting, overseeing, and reporting non-clinical safety studies (GLP and non-GLP) to support drug development and regulatory submissions.
Role type
Senior IC study director (toxicology)
Builds
Non-clinical safety study data for regulatory submissions
Domain
Pharmaceutical R&D and agrochemical testing
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
repeat-dose toxicity study design, teratology study design, reproductive toxicity study design, GLP compliance, regulatory guideline knowledge, scientific writing, data analysis, scientific interpretation
Preferred skills
pharmaceutical R&D process knowledge, agrochemical testing process knowledge, team leadership, multi-project management
Technologies
GLP compliance frameworks
Responsibilities
Designing non-clinical safety studies, conducting non-clinical safety studies, overseeing non-clinical safety studies, reporting non-clinical safety study results, ensuring regulatory compliance, leading study teams
Seniority
Senior, hands-on IC
