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, but few options.

Neurocrine Biosciences is a leading neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs, but few options. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine, and neuropsychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, 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 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, visitneurocrine.com, and follow the company on LinkedIn, X (Formerly Twitter) and Facebook. (*in collaboration with AbbVie)

About the Role:

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• Lead project teams in the capacity of supporting application implementation, administration, and support

• Partners with department leadership to ensure successful implementation of data management/interface tools. This will include both regulatory and validation requirements for all Clinical/Regulatory data management projects

• Provide technical support for the management of data from multiple sources and databases for the eventual submission to multiple regulatory agencies

• Interact with Clinical and Regulatory departments on issues relating to electronic submissions

• Take the lead on evaluating and implementing additional technologies that may improve the overall quality of systems throughout all departments

• Consult with department representatives to determine requirements for data access, reports, and interfaces

• Drives process improvements and efficiency and develops processes required for the successful implementation of key software systems

• Other duties as assigned

• BS/BA degree in computer science, IT, or similar field and 8+ years of IT experience; working in a pharmaceutical company with exposure to FDA regulations preferred. Recent experience implementing and in support of business applications, including Microsoft applications, preferred utilizing some or all 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. Experience supporting validated applications for regulatory purposes in a biotech/pharmaceutical company preferred. Some experience with web application technology, electronic document management systems, electronic publishing systems for regulatory filings, and exposure in database technologies and data warehousing/data mining a plus OR

• Master's degree in computer science, IT, or similar field and 6+ years of similar experience noted above

• PMP certification or working towards certification highly desired

• Has knowledge of best practices in the functional discipline and familiarity with the broader underlying concepts of related business disciplines

• Works to improve tools and processes within functional area

• Developing reputation inside the company as it relates to area of expertise

• Ability to work as part of and lead multiple teams

• Exhibits leadership skill and ability, typically leads lower levels and/or indirect teams

• Excellent computer skills

• Excellent communications, problem-solving, analytical thinking skills.

• Sees broader picture, impact on multiple departments/divisions

• Ability to meet multiple deadlines across a variety of projects/programs, with a high degree of accuracy and efficiency

• Excellent project management skills

• Must be 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

• Advance 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

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Neurocrine Biosciences is an EEO/AA/Disability/Vets employer.

We are committed to building a diverse, equitable, and inclusive workplace, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don't line up to exactly what we have outlined in the job description.

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