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Regulatory Toxicology Consultant
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- Our pipeline is comprised of two experimental drugs targeting solid tumors: CRB-701, a next-generation antibody drug conjugate (“ADC”) that targets the expression of Nectin-4 on cancer cells to release a cytotoxic payload and CRB-601, an anti-integrin monoclonal antibody that blocks the activation of TGFβ expressed on cancer cells.
- This person will be responsible for designing in vitro or in vivo nonclinical toxicology/research studies, analyzing study data, and addressing issues related to human safety.
- The person is also responsible for writing the safety pharmacology and toxicology sections of regulatory documents (IND/CTA/IB/NDA/MAA).
- Design, plan, prioritize and conduct experiments through CROs for safety pharmacology and toxicology or investigative studies of drug candidates in laboratory animals in support of Corbus discovery and development programs.
- Analyze and interpret the in vitro and in vivo study data, provide the project team on risk assessment and issue management, including support of clinical study protocol development for human safety and efficacy trials.
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