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Senior Or Principal Consultant, Nonclinical
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Full-time
- The incumbent will have a Ph. D. preferably in Toxicology with previous experience at the Food and Drug Administration coupled with a broad base of product expertise to specifically include oncology products.
- This is a ‘remote work’ position however, the incumbent will be required to travel to Alexandria, VA headquarters up to twice per year for team meetings.
- Serve as an expert in regulatory pharmacology/toxicology while providing direct consultation with biopharmaceutical companies to advise them on best approaches that will effectively advance drug development efforts from product development, provide ongoing support through early clinical stages through commercialization.
- Evaluation of nonclinical pharmacology and toxicology data.
- Design of IND-enabling nonclinical/toxicology packages and authoring study synopses.
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