Who We Are:Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in patients with Prader-Willi syndrome, 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 more than 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, Facebook and YouTube. (*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._Your Contributions (include, but are not limited to):Serves as the primary project team representative, delegating work as appropriateGenerates SDTM domains, ADaM data sets, and Define.xml files with proficiency in creating specification files for these domainsGenerates analysis data sets, tables, figures, and listings to support the analysis of clinical trials dataReviews output across programs to ensure consistencyReviews maintains and approves study documents per standard proceduresProvides programming support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requestsPrograms, tests, and documents global utility programs and tools in accordance with standards and validation proceduresProvides technical expertise to the development of programming standards and procedures, technical expertise in the areas of analysis and reportingParticipates in the development and/or maintenance of departmental procedures and standardsPerforms programming using techniques such as macro language, advanced data manipulation, and statistical proceduresImplements data management plans designed to meet project and protocol deadlinesActs as a liaison between clinical management, subcommittees and project teams as neededMay train and mentor new programmersPerforms other duties as assignedRequirements:BS/BA degree in computer science, mathematics, statistics, or related discipline AND 4+ years experience in the Biopharmaceutical (or CRO) industry as a statistical programmer with advanced knowledge of SAS, (Base, Stat, Macro, graph). In addition, must have at least three years of experience serving in a supervisory or lead capacity. Experience managing projects ORMaster’s degree in computer science, mathematics, statistics, or related discipline AND 2+ years of similar experience noted above ORPhD in computer science, mathematics, statistics, or related discipline AND similar experience as noted aboveUnderstands key business drivers and uses this understanding to accomplish workHas strong understanding of processes, procedures and systems used to accomplish the work and recognizes downstream impact on other functional areasProficient with tools and processes that support work conducted by functional areaAbility to work as part of a team; may train lower levelsExcellent computer skillsStrong communications, problem-solving, analytical thinking skillsDetail oriented yet can see broader picture for departmentAbility to meet multiple deadlines, with a high degree of accuracy and efficiencyStrong project management skillsStrong interpersonal skills to effectively work in a team environmentExcellent organizational skills, time management, and ability to coordinate workload and meet established deadlinesProficiency with Word, Excel, and PowerPoint is required as is the ability to communicate effectively both verbally and in writingDemonstrates strong knowledge with industry standards, such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelinesStrong programming skills in SAS, (Base, Stat, Macro, graph), R, STAT or similarStrong knowledge of SDTM domains, ADaM data sets, and Define.xml files with proficiency in creating specification files for these domainsStrong knowledge of writing, validating, and documenting statistical programs, and of creating integrated programming libraries and systemsStrong understanding of relational databases and experience working with complex data systemsWe will make multiple hires at this level.#LI-SA1Neurocrine 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._The annual base salary we reasonably expect to pay is $110,800.00-$151,000.00. 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.