Fractional Toxicology Consultant
FoundationsStephen· hybrid
Provides nonclinical safety consultancy to drug development organizations navigating complex regulatory pathways.
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The work I do
regulatory toxicology and nonclinical safety for drug development
Problems I solve
- Identify gaps in your nonclinical development plan
- Help identify and provide oversight of studies at the right CRO for your pivotal studies
- Drive your nonclinical development strategy to get you ready for regulatory submissions
- Troubleshoot issues in your nonclinical safety package and provide a way forward
Who I work with
biopharmaceutical companies, CROs, and drug manufacturers needing expertise in nonclinical safety and regulatory compliance
What I bring
- expertise in regulatory toxicology and immunotoxicology, applied in various capacities across North America and the UK
- 20 years of GLP experience, gained working in multiple nonclinical CROs
- specialization in biopharmaceutical and immunomodulatory therapeutics and vaccines, demonstrated in drug development and safety assessments
Commercial
- £800 / day