Cambridge, United Kingdom
Are you a highly motivated nonclinical safety scientist with extensive experience in the pharmaceutical industry? If so, then we want to hear from you. We are looking for a talented nonclinical safety expert to head up our Nonclinical Safety department at Director grade, providing significant support to our portfolio of small molecule drug discovery programs.
Based at our London or Cambridge offices and with flexible working arrangements, you will have accountability for all nonclinical safety activities across the portfolio, defining the safety strategy to progress programs through drug discovery and development.
Lead, mentor, and manage a small team of nonclinical safety scientists
Represent safety pharmacology on the drug discovery leadership team
Provide expert guidance to project teams, taking accountability for decision making and defining industry-leading approaches to address safety issues at all stages of development from target ID to preclinical development
Design and implement robust toxicology studies to assess the safety profile of drug candidates, ensuring compliance with regulatory guidelines
Define comprehensive and actionable safety derisking strategies from target ID onwards, integrating target safety assessments, in silico toxicology and the latest in vitro toxicology methods
Collaborate with cross-functional teams, contributing to the overall drug discovery and development strategy
Provide nonclinical safety expertise to define indication specific regulatory strategy and take responsibility for regulatory submission authoring
Keep up to date with industry trends, regulatory requirements, and advancements in nonclinical safety and drug development
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