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Senior Statistical Programmer Jobs (NOW HIRING)

Fortrea

Senior Statistical Programmer

San Jose, CA · Remote

Perform the role of the Lead Statistical Programmer. * Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, working within budget ...

Syneoshealth

OR · On-site

Sr Statistical Programmer (NA Only) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point ...

Atorus Research

Sr R & SAS Programmer

Chesterbrook, PA · On-site

Sr SAS & R Programmer onsite in the Chesterbrook, PA area 3 days/week SUMMARY The contract Senior Statistical Programmer is a member of the Biometrics Department within the Research and Development ...

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How much do senior statistical programmer jobs pay per year?

As of Jun 12, 2026, the average yearly pay for senior statistical programmer in the United States is $128,293.00, according to ZipRecruiter salary data. Most workers in this role earn between $107,000.00 and $148,000.00 per year, depending on experience, location, and employer.

What is a Senior Statistical Programmer job?

A Senior Statistical Programmer is responsible for developing, testing, and validating statistical programs used for clinical trial data analysis. They work primarily with statistical software like SAS to generate tables, listings, and figures (TLFs) for regulatory submissions and research studies. This role requires strong programming skills, knowledge of statistical methodologies, and an understanding of clinical trial processes. Senior Statistical Programmers also collaborate with statisticians, data managers, and regulatory teams to ensure data integrity and compliance with industry standards.

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

To thrive as a Senior Statistical Programmer, a strong background in statistical analysis, programming (often in SAS and R), and a relevant degree such as in statistics, mathematics, or computer science is essential. Experience with regulatory submission standards (like CDISC SDTM/ADaM), clinical trial software, and certifications such as SAS Certified Advanced Programmer are highly valued. Outstanding attention to detail, problem-solving abilities, and effective communication skills help individuals excel in this collaborative and deadline-driven role. These skills are crucial for ensuring accurate data analysis, regulatory compliance, and successful teamwork in high-stakes research environments.

What are the typical responsibilities and team dynamics for a Senior Statistical Programmer?

As a Senior Statistical Programmer, you will typically be responsible for designing, developing, and validating statistical programs for clinical trial data analysis and reporting. You’ll work closely with biostatisticians, data managers, and clinical project teams to ensure data quality and regulatory compliance, often contributing to the creation of submission datasets and study reports. The role usually involves both independent work and active collaboration, with seasoned programmers frequently mentoring junior staff and participating in process improvement initiatives. This team-oriented structure offers exposure to a variety of projects and stakeholders, making it a dynamic environment ideal for those who enjoy both analytical tasks and cross-functional teamwork.

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Senior Statistical Programmer jobs near you
Infographic showing various Senior Statistical Programmer job openings in the United States as of June 2026, with employment types broken down into 20% As Needed, 20% Full Time, 20% Part Time, and 40% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $128,293 per year, or $61.7 per hour.

Senior Statistical Programmer

Hengrui Pharma

Chicago, IL

Other

Posted 15 days ago

Job description

Main Responsibilities

  1. Review and provide comments on study documents, including but not limited to, protocol, statistical analysis plan, table shell, case report form, data management plan, data verification plan, data transfer plan etc.
  2. Develop/validate and review of SDTM and ADaM data specifications.
  3. Create/validate CDISC compliant SDTM and ADaM datasets and generate tables, figures and data listings (TFLs) upon team's request.
  4. Prepare data submission packages including aCRF, xpt files, define.xml, reviewer's guides, computer programs and other documents, etc.
  5. Archive relevant documentation and deliverables.
  6. Works closely with other programmers to ensure the quality of all deliverables and project timelines are met.
  7. Ensure that all departmental standard operating procedures that govern any aspect of their work are adhered to.
  8. Contribute to process improvement initiatives.


Work Location:

Guangzhou, China or Suzhou, China


Qualifications:

Education: Bachelor's or higher degree in a statistic, mathematics, computer science, life sciences or health-related field. Experience in a pharma, biotech, or CRO environment is preferred.


Experience:

Knowledge/experience of data structures and relevant programming languages (e.g., SAS, R, Python, etc) for data manipulation and reporting. Knowledge of Visual Basic, Java, C#, or Perl programming language is preferred.


Language Requirement: Fluent in both written and verbal communication in English.


Other Skills:

  • Strong capability on self-learning, independent thinking and problem solving.
  • Good teaming collaboration. Able to work under high pressure.

Good interpersonal and communication skills.

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