Neurocrine Biosciences
Analyst, Statistical Programming - (San Diego based)
Neurocrine Biosciences, San Diego, California, United States, 92189
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
Performs statistical analysis on data supporting the SAS statistical programming efforts for clinical and non-clinical projects and studies, including developing, testing, maintaining, validating, and documenting SAS programs to evaluate clinical data and meet the project’s needs.
Your Contributions (include, But Are Not Limited To)
Generates analysis data sets, tables, figures, and listings to support the analysis of clinical trials dataGenerate SDTM domains, ADaM datasets, and Define.xml filesAssists in creation of table mock-ups under supervision of statisticiansReviews output across programs to ensure consistency. Recognizes inconsistencies and initiates resolution of data problemsTypically creates programs using statistical analysis system language to support the clinical areaPerforms programming using techniques such as macro language, advanced data manipulation, and statistical proceduresImplements data management plans designed to meet project and protocol deadlinesProvides expertise in the design and development of clinical trials, protocols and case report formsActs as a liaison between clinical management, subcommittees and project teams as neededPerforms other duties as assignedRequirements
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 ORMaster’s degree in Statistics, Mathematics, or Computer Science or in a related field and some experience noted aboveKnowledge of Biotechnology/Pharmaceutical/CRO industry, specifically clinical trial SAS programming, CDISC data structuresStrong knowledge of statistical programming tools such as STAT, R, SASDemonstrates knowledge of industry standards, such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelinesDemonstrated organizational skills, time management, and ability to coordinate workload and meet established deadlinesStrong communication and interpersonal skills to effectively work in a team environment under the direction of a lead programmer and statisticianTechnical knowledge of SDTM, ADaM, and Define.XMLUnderstands Neurocrine's business objectives and developing understanding of Neurocrine's services and customersHas experience in specific functional discipline while working to acquire higher-level knowledge and skillsComfortable with tools and processes that support work conducted by functional areaAbility to work as part of a teamStrong computer skillsGood communications, problem-solving, analytical thinking skillsDetail orientedAbility to meet deadlinesGood project management skillsNeurocrine 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 $86,200.00-$125,050.00. 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.#J-18808-Ljbffr
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
Performs statistical analysis on data supporting the SAS statistical programming efforts for clinical and non-clinical projects and studies, including developing, testing, maintaining, validating, and documenting SAS programs to evaluate clinical data and meet the project’s needs.
Your Contributions (include, But Are Not Limited To)
Generates analysis data sets, tables, figures, and listings to support the analysis of clinical trials dataGenerate SDTM domains, ADaM datasets, and Define.xml filesAssists in creation of table mock-ups under supervision of statisticiansReviews output across programs to ensure consistency. Recognizes inconsistencies and initiates resolution of data problemsTypically creates programs using statistical analysis system language to support the clinical areaPerforms programming using techniques such as macro language, advanced data manipulation, and statistical proceduresImplements data management plans designed to meet project and protocol deadlinesProvides expertise in the design and development of clinical trials, protocols and case report formsActs as a liaison between clinical management, subcommittees and project teams as neededPerforms other duties as assignedRequirements
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 ORMaster’s degree in Statistics, Mathematics, or Computer Science or in a related field and some experience noted aboveKnowledge of Biotechnology/Pharmaceutical/CRO industry, specifically clinical trial SAS programming, CDISC data structuresStrong knowledge of statistical programming tools such as STAT, R, SASDemonstrates knowledge of industry standards, such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelinesDemonstrated organizational skills, time management, and ability to coordinate workload and meet established deadlinesStrong communication and interpersonal skills to effectively work in a team environment under the direction of a lead programmer and statisticianTechnical knowledge of SDTM, ADaM, and Define.XMLUnderstands Neurocrine's business objectives and developing understanding of Neurocrine's services and customersHas experience in specific functional discipline while working to acquire higher-level knowledge and skillsComfortable with tools and processes that support work conducted by functional areaAbility to work as part of a teamStrong computer skillsGood communications, problem-solving, analytical thinking skillsDetail orientedAbility to meet deadlinesGood project management skillsNeurocrine 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 $86,200.00-$125,050.00. 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.#J-18808-Ljbffr