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Director Toxicology
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$225,000 - $260,000 a year
Full-time
- The Director of Toxicology will serve as the primary point of contact between global project teams and Nonclinical Drug Safety (NDS) and is responsible for developing nonclinical safety strategies that support the clinical development plan in oncology, metabolic, and additional non-oncology indications.
- Conduct In-Vivo Pharmacokinetic, Pharmacodynamic and Toxicology study design and data review, serving as the main point of contact for receiving, reviewing, and interpreting study data.
- Compile and convey all report comments to the Study Director at the TPO.
- Collaborate with cross-functional departments (including Research, Pharmacology, DMPK, Translational Medicine & Clinical Pharmacology, CMC, Regulatory Affairs, Patient Safety and Pharmacovigilance) to implement discovery & development of toxicology strategies to enable the progression of optimized drug candidates and ensure that toxicological considerations are integrated into all stages of product development.
- Act as the company toxicology representative on external pre-clinical safety related consortia, addressing questions in interactions with FDA, EMA and other authorities on preclinical safety topics.
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