Director, Toxicology

Company Overview Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. We are advancing an innovative portfolio of therapeutics, supported by a leadership team with deep experience in the design, development, and commercialization of cutting-edge therapies, including antibody-drug conjugates. Our pipeline includes varegacestat, an investigational gamma secretase inhibitor for which an NDA has been accepted by the U.S. FDA; IM-1021, a clinical-stage ROR1 ADC; IM-1617, a clinical-stage solid tumor ADC; and IM-3050, a clinical-stage FAP-targeted radioligand therapy. We are also advancing a broad portfolio of early-stage ADCs pursuing undisclosed solid tumor targets. Position Overview The Director, Toxicology provides scientific and strategic leadership for the nonclinical safety assessment of oncology therapeutics from discovery through commercialization. This individual serves as the toxicology lead on multidisciplinary project teams and is responsible for developing scientifically rigorous, phase-appropriate nonclinical safety strategies that enable efficient progression of pipeline assets while meeting global regulatory expectations. The Director partners closely with Research, Clinical Development, Translational Science (DMPK, Biomarkers), Regulatory Affairs, CMC, Biometrics, Pathology, and external CROs to design and execute toxicology programs supporting INDs, CTAs, BLAs, NDAs, lifecycle management activities, and responses to health authorities. The successful candidate combines deep scientific expertise with strategic judgment to identify and mitigate development risks while advancing innovative oncology therapeutics. Responsibilities Scientific Leadership Serve as the nonclinical safety lead for multiple oncology development programs from candidate selection through regulatory approval . Develop integrated, phase-appropriate nonclinical safety strategies that support efficient clinical development while meeting global regulatory expectations . Provide scientific leadership on target-, platform-, and modality-related safety risks and develop mitigation strategies . Lead interpretation of complex toxicology findings and translate results into actionable recommendations for project teams and executive leadership . Integrate toxicology, pharmacology, DMPK, pathology, biomarker, and clinical data into comprehensive benefit-risk assessments . Regulatory Strategy Design nonclinical development plans supporting INDs, CTAs, NDAs, BLAs, and global regulatory interactions . Author and review nonclinical sections of regulatory submissions including INDs, Investigator's Brochures, CTDs, briefing packages, orphan drug applications, pediatric plans, and responses to regulatory questions . Represent Toxicology during FDA, EMA, PMDA, and other global health authority interactions . Ensure nonclinical programs comply with ICH, FDA, EMA, OECD, and applicable global regulatory guidance . Study Oversight Design, oversee, and interpret GLP and non-GLP toxicology studies conducted at external CROs . Provide scientific oversight of study protocols, amendments, pathology peer review, data interpretation, and final reports . Oversee study monitoring activities to ensure high-quality execution and data integrity . Manage CRO performance, timelines, budgets, and scientific deliverables . Cross-Functional Leadership Represent Toxicology on cross-functional project teams . Partner with Clinical Pharmacology, Translational Sciences (DMPK, Biomarkers), Regulatory Affairs, CMC, Clinical Development, Biometrics, and Research to optimize development strategies . Communicate complex scientific issues effectively to technical and executive audiences . Mentor junior scientists and contribute to development of departmental capabilities and scientific standards . Innovation Identify opportunities to incorporate emerging technologies including AI-enabled data analysis, predict…