Job Description

Who We Are: At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs. What We Do: Neurocrine Biosciences is a leading neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine, and neuropsychiatric disorders. Our portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, endometriosis* and uterine fibroids*, as well as a pipeline with multiple compounds in clinical development across our core areas. For three decades, we have applied our neuroscience insights to treat complex conditions, relentlessly pursuing medicines to ease the burden of debilitating diseases because you deserve brave science. For more information, visit neurocrine.com and follow us on LinkedIn, X, and Facebook. ( *in collaboration with AbbVie ) About the Role: This role involves overseeing the design, conduct, interpretation, and reporting of Safety Pharmacology and Toxicology studies for Discovery and Development programs. The candidate will collaborate with preclinical colleagues to develop Safety Pharmacology and Toxicology strategies, represent Preclinical Development on teams, and interface with internal and external colleagues to ensure timely dissemination of findings. The role also includes authoring and reviewing regulatory submissions and meeting with Health Authorities to support clinical trials from First in Human to phase 3 and marketing applications. Your Contributions (include, but are not limited to): Drive the strategic scientific direction for assigned programs. Lead design, conduct, interpretation, and reporting of Safety Pharmacology and Toxicology studies. Align Toxicology responsibilities with portfolio priorities and ensure timely completion. Manage studies at CROs. Evaluate toxicology and safety pharmacology results, communicate findings, and advise on their impact. Author and review summaries for clinical and regulatory documents. Represent Preclinical Development on teams. Interface with scientists to disseminate safety study results. Contribute to SOPs and oversee adherence to Toxicology SOPs. Manage junior department members. Perform other tasks as assigned. Requirements: PhD or equivalent with 7+ years relevant experience and management experience. Deep knowledge of the functional area, strategies, and company goals. Ability to lead multiple teams and drive strategic planning. Strong leadership, mentoring, communication, problem-solving, and project management skills. State-of-the-art knowledge of practices and technologies. Excellent data evaluation, summarization, and communication skills. Ability to effectively present to diverse audiences, including regulators. Understanding of scientific literature outside immediate expertise. Experience preparing regulatory manuscripts and familiarity with guidance (ICH, EMA, FDA). Neurocrine Biosciences is an EEO/Disability/Vets employer, committed to a workplace of belonging, respect, and empowerment. We encourage candidates to apply regardless of experience gaps relative to the outlined qualifications. The annual base salary ranges from $177,100 to $256,350, with additional bonuses, equity incentives, and comprehensive benefits, including retirement, paid leave, and health coverage. #J-18808-Ljbffr Neurocrine Biosciences

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