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    Principal Analyst, Systems - San Diego, United States - Neurocrine Biosciences

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    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, but few options.

    What We Do:

    Neurocrine Biosciences is a 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, endocrine and psychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, Parkinson's disease, endometriosis* and uterine fibroids*, as well as clinical programs in multiple 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. *in collaboration with AbbVie

    About the Role:
    Leads efforts to maintain and improve a robust and state of the art research software environment. Plans and directs the analysis of complex business problems to be solved with automated systems. Supports application management for research and development. Manages application implementation projects with accountability for budget and project delivery. Provides technical direction in identifying, evaluating and developing systems and procedures that are cost-effective and meet user requirements. Configures system settings and options; plans and executes unit integration and acceptance testing; and creates specifications for systems to meet business requirements. Determines system specifications and working parameters for hardware/software compatibility. Designs details of automated systems. May provide consultation to users in the area of automated systems. May lead cross-functional linked teams to address business or systems issues.

    Your Contributions (include, but are not limited to):
    • Leads development projects for systems (LIMS or similar) data tracking; including technical requirements evaluation for new software system projects
    • Develops solutions for integration of novel research software systems
    • Represents team on large interdisciplinary teams
    • Proactively monitors, troubleshoots more complex issues and implements improvements for already in place data systems
    • Manages end-user software documentation and owns enhancements to data workflow processes
    • For all areas, leads, trains and mentors less experienced team members
    • Interacts with relevant departments on issues relating to production environments, enhancements and release management
    • Takes the lead on evaluating and implementing additional technologies that may improve the overall quality of systems throughout department
    • Consults with scientific/business representatives to determine requirements for data access, reports, and interfaces and maintains interaction with department managers to ensure successful implementation of data management/interface tools
    • Evaluates and recommends process improvements and supports the development of processes required for the successful implementation of key software systems
    • Participates on project teams in the capacity of supporting application implementation, administration, and support
    • Other duties as assigned
    Requirements:
    • BS/BA degree in computer science or IT and 6+ years of IT experience working in a pharmaceutical company with exposure to FDA regulations. 5+ years of IT experience with 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. Experience supporting validated applications for regulatory purposes in a biotech/pharmaceutical company strongly required OR
    • Master's degree in computer science or IT preferred and 4+ years of similar experience noted above
    • 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
    • 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
    #LI-SA1

    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.

    The annual base salary we reasonably expect to pay is $125,700.00-$182, 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 30% 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.

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