Senior Scientist II, Toxicologist

Role: Senior Scientist 2 in Pharmacology and Toxicology supporting nonclinical development of small molecule and biologic therapeutics for rare genetic diseases. Primary objectives include designing, implementing, and interpreting nonclinical pharmacology and toxicology studies across all drug development stages, from late research to market applications. Responsibilities encompass preparing regulatory documents, collaborating with CROs and internal teams, supporting regulatory interactions (e.g., IND/CTA submissions), and providing scientific leadership in cross-functional project teams. Requirements: Ph.D. in toxicology, pharmacology, or related field; 5+ years of industry experience in nonclinical pharmacology/toxicology within pharma, biotech, or CROs; solid understanding of drug development processes, GLPs, and regulatory standards; experience with small molecules and biologics; strong communication and collaboration skills. Preferred: Board certification in Toxicology. High-value specifics include supporting therapeutics for rare genetic conditions via small molecules and biologics, with involvement in GLP toxicology studies, regulatory submissions, and global regulatory interactions (FDA, EMEA, MHRA). Work setup details are not specified, but the role involves cross-functional collaboration, scientific reporting, and potential external partnerships.