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 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:

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

• Generate SDTM domains, ADaM datasets, and Define.xml files

• Assists in creation of table mock-ups under supervision of statisticians

• Reviews output across programs to ensure consistency. Recognizes inconsistencies and initiates resolution of data problems

• Typically creates programs using statistical analysis system language to support the clinical area

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

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

• Provides expertise in the design and development of clinical trials, protocols and case report forms

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

• Performs other duties as assigned

• BS/BA degree in Statistics, Mathematics, or Computer Science or in a related field and 2+ years of Biotechnology/Pharmaceutical/CRO industry experience as a clinical trial SAS Programmer programming CDISC data structures OR

• Master's degree in Statistics, Mathematics, or Computer Science or in a related field and Some experience noted above

• Understands Neurocrine's business objectives and developing understanding of Neurocrine's services and customers

• 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

• Ability to work as part of a team

• Strong computer skills

• Good communications, problem-solving, analytical thinking skills

• Detail oriented

• Ability to meet deadlines

• Good project management skills

• Knowledge of Biotechnology/Pharmaceutical/CRO industry, specifically clinical trial SAS programming, CDISC data structures

• Strong knowledge of statistical programming tools such as STAT, R, SAS

• Demonstrates knowledge of industry standards, such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines

• Demonstrated organizational skills, time management, and ability to coordinate workload and meet established deadlines

• Strong communication and interpersonal skills to effectively work in a team environment under the direction of a lead programmer and statistician

• Technical knowledge of SDTM, ADaM, and Define.XML

#LI-TM1

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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