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Sas Statistical Programmer Jobs (NOW HIRING)

Gilead Sciences, Inc.

Statistical Programmer II

$107K - $138K/yr

Demonstrates SAS programming proficiency. * Generates the production of statistical analysis datasets and outputs (e.g., tables, figures, and listings) for study reports and integrated summaries.

Collabera

SAS Programmer

Jersey City, NJ

The role of the Senior Statistical Programmer is to perform statistical programming activities for ... with SAS in a pharmaceutical or CRO environment Bachelor's Degree or above in Statistics ...

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How much do sas statistical programmer jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for sas statistical programmer in the United States is $57.37, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $85.34 per hour, depending on experience, location, and employer.

What types of projects do Sas Statistical Programmers typically work on, and how do they collaborate with other teams?

Sas Statistical Programmers often work on projects involving the analysis and reporting of clinical trial or observational study data, producing datasets, tables, listings, and figures to support regulatory submissions or scientific publications. They routinely collaborate with biostatisticians, clinical data managers, and project managers to ensure data quality and compliance with industry standards. Daily responsibilities include coding in SAS, validating datasets, troubleshooting data issues, and preparing documentation. Effective communication and teamwork are essential, as the role frequently involves working in multidisciplinary teams to meet project goals and timelines.

What is a SAS Statistical Programmer job?

A SAS Statistical Programmer is a professional who utilizes SAS software to manage, analyze, and report statistical data, primarily in industries like pharmaceuticals, healthcare, and clinical research. They write and validate programs to generate tables, listings, and figures for clinical trials or other data-driven studies. Their role involves ensuring data accuracy, compliance with regulatory guidelines, and collaboration with statisticians and researchers to support decision-making.

What are the key skills and qualifications needed to thrive in the Sas Statistical Programmer position, and why are they important?

To thrive as a Sas Statistical Programmer, you need a strong background in statistics, programming (especially SAS), and data management, usually supported by a degree in statistics, computer science, or a related field. Familiarity with SAS Base, SAS Macro, and clinical data standards like CDISC, as well as relevant industry certifications, are commonly required. Attention to detail, strong problem-solving abilities, and effective communication skills are valuable soft skills. These competencies ensure accurate data analysis, clear reporting, and successful collaboration within cross-functional teams in fields like healthcare or pharmaceuticals.

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Sas Statistical Programmer jobs near you
Infographic showing various Sas Statistical Programmer job openings in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 83% Physical, 3% Hybrid, and 14% Remote job distribution, with an average salary of $119,333 per year, or $57.4 per hour.
Sr. Principal Analyst, Statistical Programming

Sr. Principal Analyst, Statistical Programming

Neurocrine Biosciences, Inc.

San Diego, CA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 25 days ago

Job 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.
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:
Leads major statistical programming efforts for clinical program area of responsibility. Develops and recommends system capabilities roadmap for in-house development and external vendor selection process. Acts as a system expert in designing, developing, testing, maintaining, validating, and documenting SAS programs to evaluate clinical data and meet the project requirements for SAS statistical programming efforts. Provides expert-level technical advice for all aspects of the program development process, tools and software, standards and procedures.
Your Contributions (include, but are not limited to):
  • Provides expert technical leadership across multiple functions serving as the key representative for Biometrics
  • Contributes to the development of Biometrics functional strategy and serves as system expert for Statistical Programming efforts
  • Leads and mentors a team of statistical programmers to support the analysis and reporting of data from clinical and nonclinical studies for all corporate development programs
  • Leads end-to-end statistical programming work-streams on multidisciplinary program teams company-wide
  • Provides technical direction in the development and implementation of programming standards and conventions, building statistical programming infrastructure
  • Provides workforce planning recommendations based on project workloads in order to ensure appropriate programming resources are available to complete tasks in a timely manner
  • Manages vendor selection processes and validates vendor programming activities such as CDISC implementation, analysis reporting, and programming conventions
  • Supports creation and validation of e-submission requirements (i.e. annotated CRF, datasets files, define documents)
  • Serves as primary/lead programmer for agency reporting deliverables such as DSUR/Annual Report and IB updates
  • Performs the function of lead and/or quality control statistical programmer on projects as needed
  • Performs other duties as assigned
Requirements:
  • BS/BA degree in computer science, mathematics, statistics, or related discipline AND 8+ years in the Biopharmaceutical (or CRO) industry as a statistical programmer with advanced knowledge of SAS, (Base, Stat, Macro, graph), CDISC data structures. In addition, must have at least 2 years of experience serving in a supervisory or lead capacity. Experience managing large projects and external vendors. OR
  • Master's degree in computer science, mathematics, statistics, or related discipline AND 6+ years similar experience noted above OR
  • PhD degree in computer science, mathematics, statistics, or related discipline AND 4+ years similar experience noted above
  • Anticipates business and industry issues; recommends relevant process / technical / service improvements
  • Demonstrates broad expertise or unique knowledge
  • Considered an expert within the company and may have external presence in area of expertise
  • Applies in-depth expertise in discipline and broad knowledge of other closely related areas to improve efficiency of team
  • Ability to work as part of and lead multiple teams
  • Good leadership, mentoring skills and abilities typically leads lower levels and/or indirect teams
  • Excellent computer skills
  • Excellent communications, problem-solving, analytical thinking skills
  • Sees broader picture and longer-term impact on division/company
  • Ability to meet multiple deadlines across a variety of projects/programs, with a high degree of accuracy and efficiency
  • Excellent project management, strong project leadership skills
  • Expert knowledge of the following:
    • Developing and implementing statistical programming SOPs and processes in a clinical environment
    • Relational databases and complex data systems.
    • Industry standards, such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines
    • Programming skills in SAS, (Base, Stat, Macro, graph), R, STAT or similar
    • SDTM domains, ADaM data sets, and Define.xml files with proficiency in creating specification files for these domains
  • Knowledge of all aspects of writing, validating, and documenting statistical programs, and of creating integrated programming libraries and systems
  • Proven experience in multi-discipline, cross-functional project management in a clinical, highly regulated environment
  • Track record of success with effectively organizing and managing multiple assignments with challenging timelines across multiple personnel

#LI_SA1
Neurocrine 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 $156,900.00-$214,000.00. 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 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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