Sr. Analyst, Statistical Programming

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.

What We Do:

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)

About the Role:

Designs, develops, tests, maintains, validates, and documents SAS programs to evaluate clinical data and meet the project requirements for SAS statistical programming efforts for clinical and non-clinical projects and studies. Provides technical expertise to the development of programming standards and procedures.

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Your Contributions (include, but are not limited to):

• Serves as the primary project team representative, delegating work as appropriate

• Generates SDTM domains, ADaM data sets, and Define.xml files with proficiency in creating specification files for these domains

• Generates analysis data sets, tables, figures, and listings to support the analysis of clinical trials data

• Reviews output across programs to ensure consistency

• Reviews maintains and approves study documents per standard procedures.

• Provides programming support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests

• Programs, tests, and documents global utility programs and tools in accordance with standards and validation procedures

• Provides technical expertise to the development of programming standards and procedures, technical expertise in the areas of analysis and reporting

• Participates in the development and/or maintenance of departmental procedures and standards

• Performs programming using techniques such as macro language, advanced data manipulation, and statistical procedures

• Implements data management plans designed to meet project and protocol deadlines

• Acts as a liaison between clinical management, subcommittees and project teams as needed

• May train and mentor new programmers

• Performs other duties as assigned

Requirements:

• BS/BA degree in computer science, mathematics, statistics, or related discipline and 4+ years experience in the Biopharmaceutical (or C