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Sas Statistical Programmer Jobs (NOW HIRING)

LivaNova

Statistical Programmer II

Minneapolis, MN · On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Develop, validate, and maintain SAS programs in accordance with study requirements, internal ...

LivaNova

Statistical Programmer II

Houston, TX

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Develop, validate, and maintain SAS programs in accordance with study requirements, internal ...

LivaNova

Statistical Programmer II

Austin, TX · On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Develop, validate, and maintain SAS programs in accordance with study requirements, internal ...

LivaNova

Statistical Programmer II

Atlanta, GA · On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Develop, validate, and maintain SAS programs in accordance with study requirements, internal ...

LivaNova

Statistical Programmer II

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Develop, validate, and maintain SAS programs in accordance with study requirements, internal ...

IQVIA

Principal Statistical Programmer

Durham, NC

$98K - $273K/yr

Principal Statistical Programmer Start Date: Targeted for midJuly Position Summary We are seeking a ... Expert proficiency in base SAS and Advanced SAS with good hands on SAS Macros * Indepth knowledge ...

LivaNova, PLC

Statistical Programmer II

Atlanta, GA · On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Develop, validate, and maintain SAS programs in accordance with study requirements, internal ...

LivaNova

Statistical Programmer II

Dallas, TX · On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Develop, validate, and maintain SAS programs in accordance with study requirements, internal ...

LivaNova

Statistical Programmer II

Boston, MA

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Develop, validate, and maintain SAS programs in accordance with study requirements, internal ...

LivaNova

Statistical Programmer II

Phoenix, AZ · On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables ... Develop, validate, and maintain SAS programs in accordance with study requirements, internal ...

IQVIA

Principal Statistical Programmer

Durham, NC

$98K - $273K/yr

Principal Statistical Programmer Start Date: Targeted for midJuly Position Summary We are seeking a ... Expert proficiency in base SAS and Advanced SAS with good hands on SAS Macros * Indepth knowledge ...

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Sas Statistical Programmer information

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How much do sas statistical programmer jobs pay per hour?

As of Jul 1, 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 June 2026, with employment types broken down into 90% Full Time, and 10% Part Time. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $119,333 per year, or $57.4 per hour.

Lead statistical Programmer

Katalyst Healthcares and Life Sciences

Boston, MA • On-site

Other

Posted 8 days ago

Job description

Job Summary:
The Contract Lead Programmer serves as a senior, hands-on programmer responsible for managing statistical programming activities across multiple clinical trials and therapeutic areas. The role oversees external CRO partners to ensure high-quality, timely, and compliant delivery of analysis datasets, tables, listings, and figures that support clinical development and regulatory submissions. The position involves hands-on technical leadership and requires comprehensive and detailed knowledge of statistical programming languages and software, filing support, clinical trial databases, and the drug development process.
Responsibilities:
  • Lead statistical programming activities and deliverables (e.g., SDTM/ADaM datasets, tables, listings, figures, review esub data packages with Pinnacle 21) across multiple studies and programs, serving as the primary programming point of contact. Must be able to review TMF for programming deliverables, including SAP.
  • Oversee CRO programming activities by reviewing programming plans, SDTM/ADaM specifications, TLF shells, validation strategies, and issue logs.
  • Monitor internal and CRO delivery against timelines, quality metrics, and contractual obligations; identify risks and implement mitigation or corrective actions as needed.
  • Ensure consistency of standards, templates, macros, and processes across internal and external teams, and drive adoption of programming best practices.
  • Provide hands-on programming support to complex or high-priority analyses, ad-hoc requests, and regulatory responses, as needed.
  • Partner with biostatistics to design, implement, and maintain programming development plans for each project, ensuring timely and high-quality deliverables aligned with internal and industry standards.
  • Partner with data management to apply CDISC standards during CRF design and database development.
  • Partner with biostatistics, data management, clinical, regulatory, pharmacovigilance, and project management to align programming strategies with study-level plans and regulatory expectations.
  • Collaborate with medical writing, clinical, and regulatory on study-level initiatives.
  • Support inspection and audit readiness by ensuring appropriate documentation, traceability, and reproducibility of programming deliverables from both internal and CRO teams.
Requirements:
  • Master's degree (or equivalent experience) in statistics, computer science, mathematics, or a related field.
  • 10+ years of programming experience in the pharmaceutical, biotechnology, or CRO industry.
  • 3-5 years of experience as a lead programmer in statistical programming and CRO oversight.
  • Proven record in developing and implementing statistical programming standards and procedures.
  • In-depth knowledge of CDISC (CDASH, SDTM, ADaM) standards and regulatory submission requirements.
  • dvance proficiency in Base SAS, SAS/STAT, SAS Macro language, and SAS SQL; SAS/GRAPH a plus (SAS version 9 or higher).
  • Proficient in coding, debugging, and optimizing new and existing programs.
  • Experience leading studies and supporting NDA and EMEA submissions.
  • daptable, detail-oriented, effective under pressure with initiative to take on new challenges.
  • Demonstrated ability to establish and articulate a plan for a team to ensure appropriate focus and direction.
  • Excellent analytical, problem-solving, organizational, and multitasking abilities.
  • Excellent communication and interpersonal skills, both verbal and written.
  • Collaborative team player with a customer-focused mindset; strives to support others to succeed.
  • bility to communicate technical information to non-scientists, and willingness to educate the internal team.
  • Committed to quality and maintaining a positive attitude under shifting priorities.
  • bility to contribute to strategic planning for data standards, system infrastructure, and process optimization initiatives.

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