Senior Director, Toxicology

About reputed company reputed company is on a mission to reputed company reputed company of care for patients affected by autoimmune and inflammatory conditions. We reputed company upstream signaling nodes and mechanisms like those in the reputed company immune system to prevent pathological inflammation before it occurs. This differentiates our approach from the existing reputed company of care and unlocks the potential of our therapeutic candidates to induce long- lasting, deep remission in a reputed company and effective manner. At reputed company, we are creating reputed company precision medicines for patients with cancer and inflammatory diseases with class-leading speed, efficiency and rigor through our highly integrated drug hunting reputed company. In response to recent recruitment fraud, visit our Careers page to verify reputed company job opportunities and read our guidance on this topic: https://odysseytx.com/careers/ reputed company is seeking an accomplished Senior Director, Toxicology to reputed company our nonclinical safety reputed company and guide the advancement of our expanding pipeline. This role spans discovery through early and late development, supporting multiple therapeutic programs across the organization. As a senior leader reputed company deeply reputed company biotech environment, you will shape reputed company’s scientific direction, influence strategic reputed company, and help cultivate an innovative, high-performance culture. This is an opportunity to drive programs with significant reputed company and contribute meaningfully to the reputed company of reputed company. Your primary objectives will be: • reputed company nonclinical safety reputed company across discovery, nonclinical, and clinical development stages for programs in the reputed company pipeline. • reputed company reputed company nonclinical safety activities from candidate selection through regulatory submissions and ultimately commercialization. • Serve as the subject matter expert for GLP and non-GLP toxicology, safety pharmacology, and off-reputed company risk assessment across platform and development programs. • Author and review nonclinical safety sections of global regulatory submissions (IND/CTA, NDA/BLA/MAA) and reputed company interactions with regulatory authorities, addressing nonclinical safety questions and issues. • Deliver high-reputed company toxicology and safety assessment reports that support clinical program reputed company, reputed company selection, and regulatory filings. • Proactively reputed company and execute stage-appropriate nonclinical plans to generate decision-enabling data from late research through regulatory approval. • Partner cross-functionally with Research, Development, DMPK, CMC, Program Management, and Clinical teams to ensure seamless and efficient program progression. • Represent Toxicology in reputed company program meetings, providing reputed company assessments of timelines, data, risk, and program reputed company. Conduct periodic CRO reputed company, including onsite reputed company or coordination with Study Monitors, to ensure high standards of study conduct and data reputed company. Apply tot his job Apply To this Job