Principal Scientist, Toxicologist/Study Director

Principal Scientist, Toxicologist/Study Director Key Responsibilities Serve as Study Director (single point of control) for assigned acute through chronic general toxicology studies across all modalities; ensure compliance with protocol/amendments, SOPs, regulations, safety guidelines, and company policies. Critically analyze and interpret data; integrate clinical pathology, pathology, and toxicokinetics into written reports for regulatory submissions; communicate results on timeline. Ensure regulatory rigor, proactive risk identification, and timely study execution. Participate on cross-functional teams to investigate mechanisms of toxicity. Represent nonclinical safety on product development teams; oversee strategy/design of nonclinical safety studies and develop regulatory strategies and communications with global agencies. Demonstrate enterprise mindset and strategic thinking; collaborate to deliver solutions and contribute to an inclusive environment. Deliver high-quality results with accountability and agility; continuously improve and support larger initiatives. Education PhD and/or DVM with graduate/post‑graduate training in toxicology, pharmacology, or related discipline. Requirements 8+ years as a Toxicologist or Study Director in pharma/biotech/CRO. Demonstrated experience with GLP (US FDA 21 CFR Part 58). Strong collaboration and communication across cross‑functional teams; leadership and mentoring. Clear verbal and written communication (presentations/meetings). Expertise in immunology and/or biologics, including regulatory requirements and testing. Preferred Knowledge of biotherapeutics/large‑molecule drug development strategies. Experience with outsourced study monitoring. Toxicology expert on drug discovery/development teams. Representation of nonclinical safety in regulatory agency interactions. #J-18808-Ljbffr Scorpion Therapeutics