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Key Responsibilities:
- Own nonclinical safety strategy for assigned programs, ensuring toxicology plans support candidate selection, IND-enabling development, clinical progression, and later-stage regulatory milestones.
- Design and oversee discovery, exploratory, investigative, and regulatory toxicology studies, including non-GLP and GLP studies.
- Direct CROs, consultants, and external partners, holding them accountable for scientific quality, compliance, timelines, and transparent communication.
Qualifications:
- Master's degree or PhD preferred in Toxicology, Pharmacology, Pharmacy, Biology, or related discipline; DABT certification desirable.
- 8+ years of relevant biotechnology, pharmaceutical, CRO, or regulatory agency experience.
- Deep expertise in general toxicology, regulatory toxicology, and Good Laboratory Practices.
Company Overview:
- Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into therapies for CNS disorders.
- The company values trust, ownership, curiosity, and results, and is committed to diversity, equity, and inclusion.
- Praxis offers a collaborative environment focused on advancing high-impact medicines for patients with complex brain disorders.
Praxis Precision Medicines
Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into therapies for CNS disorders. The company values trust, ownership, curiosity, and results, and is committed to diversity, equity, and inclusion.