Senior IT Program Manager

Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in Prader-Willi syndrome, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For more than three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. For more information, visit  neurocrine.com , and follow the company on  LinkedIn ,  X , Facebook and YouTube . ( *in collaboration with AbbVie ) About the Role: Operates within the Value Management Office Delivery Project & Program Management organization and supports the disciplined execution of moderately complex IT initiatives. Supports or may lead cross-functional technology projects from initiation through stabilization under broad supervision, helping ensure delivery against defined scope, schedule, budget, quality, compliance, and business outcome expectations. Partners closely with IT and business stakeholders to support effective governance, predictable execution, and alignment with established enterprise strategies and goals. Execution- and delivery-focused, emphasizing governance, risk management, stakeholder coordination, and transparent reporting to support measurable business value. _ Your Contributions (include, but are not limited to): Support or lead the execution of moderately complex IT initiatives under broad supervision Contribute to the delivery and measurement of defined business outcomes Translate defined objectives into detailed project plans, milestones, and deliverables Support adherence to regulatory, validation, and compliance requirements throughout project execution Support predictable delivery through disciplined task, risk, issue, dependency, and scope management Prepare and maintain consistent project, portfolio, and steering committee reporting Partner with IT and business stakeholders to coordinate initiative delivery with established platform roadmaps and technology plans Ensure regulatory, validation, and compliance requirements are embedded into project execution (particularly in Clinical and Regulatory systems environments) Support the tracking and reporting of defined value-realization measures Works independently to lead initiatives within the commercial organization Partners with IT Business Partners to manage the demand intake process Requirements: BS/BA degree in computer science, IT, or similar field and 4+ years of IT experience working in a pharmaceutical company with exposure to FDA regulations. Experience supporting validated applications for regulatory purposes in a biotech/pharmaceutical company required OR BS/BA degree in computer science, IT, or similar field Master’s degree in computer science, IT, or similar field and 2+ years of similar experience noted above Able to communicate technical information and work with all levels within the organization   Strong base knowledge of web application technology, electronic document management systems, electronic publishing systems for regulatory filings, and an in-depth experience in database technologies and data warehousing/data mining Strong knowledge of the most recent experience in support of Microsoft applications utilizing the following technologies: MS SQL Server, Oracle, JAVA, Visual Basic, MS Access, MS