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.
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. The company's diverse 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 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, visit neurocrine.com, and follow the company on LinkedIn, X and Facebook. (*in collaboration with AbbVie)
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Participates on project teams in a supporting capacity for application implementation, administration, and support
Reviews and assists in the development of processes required for the successful implementation of key software systems
Provides support for the management of data from multiple sources and databases for submission to regulatory agencies
Interacts with Clinical and Regulatory departments on issues relating to electronic submissions
Supports evaluation and implementation of technologies that may improve the overall quality of systems across departments
Consults with department representatives to determine requirements for data access, reports, and interfaces
May interact with department managers, typically works with main system users to assess implementation of data management/interface tools, including regulatory and validation requirements for all Clinical/Regulatory data management projects
Other duties as assigned
BS/BA degree in computer science, IT, or similar Field and 2+ years of IT experience; working in a pharmaceutical company with exposure to FDA regulations preferred
Master’s degree in computer science or IT preferred and some related experience noted above
PMP certification or working towards certification a plus
Good knowledge of Microsoft applications / data base and programming technologies
Good knowledge of with web technologies such as HTML, XML, or latest mark up language, Visual Basic / Java based or similar language and Internet Database Programming
Knowledge of validated applications for regulatory purposes in a biotech/pharmaceutical company
Familiarity with web application technology, electronic document management systems, electronic publishing systems for regulatory filings, and exposure in database technologies and data warehousing/data mining
Recent experience supporting implementation 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.
Has experience in specific functional discipline while working to acquire higher-level knowledge and skills
Comfortable with tools and processes that support work conducted by functional area
Good project management skills with ability to meet deadlines.
Ability to collaborate with a cross-functional business and technical project team.
Excellent verbal, written, and interpersonal communication skills, including the ability to work collaboratively with all employee levels as well as external contacts (vendors).
Excellent decision-making, conflict-resolution and influencing skills appropriate for a developing professional.
Neurocrine Biosciences is an EEO/Disability/Vets employer.
We are committed to building a workplace of belonging, respect, and empowerment, 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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The annual base salary we reasonably expect to pay is $81,000.00-$111,000.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 20% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.