Senior IT Program Manager

Who We Are:

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 , and follow the company on Linked In, X, Facebook and You Tube. (
* in collaboration with Abb Vie)

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.

• 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

• 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 Project, IIS, Internet Explorer, and Advanced Web technologies such as HTML, XML, SGML, Dynamic HTML, JavaScript, VBScript, and Internet Database Programming
• Strong knowledge of supporting validated applications for regulatory purposes in a biotech/pharmaceutical company required
• Understands key business drivers and uses this understanding to accomplish work
• Has strong understanding of processes, procedures and systems used to accomplish the work and recognizes downstream impact on other functional areas
• Proficient with tools and processes that support work…