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Sr 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 ...

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How much do sr statistical programmer jobs pay per year?

As of Jun 12, 2026, the average yearly pay for sr 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 are Sr Statistical Programmers?

Sr Statistical Programmers are experienced professionals who specialize in managing and analyzing complex data sets, typically in the clinical research and pharmaceutical industries. They use statistical software like SAS or R to develop and validate programs that support clinical trials, regulatory submissions, and data reporting. Their responsibilities often include ensuring data quality, creating analysis datasets, generating tables, listings, and figures, and collaborating with statisticians and data managers. Senior-level programmers also mentor junior staff and may oversee project timelines and deliverables. Their expertise is essential for turning raw clinical data into meaningful results that support drug development and regulatory decision-making.

How does a Sr Statistical Programmer typically collaborate with biostatisticians and clinical teams during a clinical trial project?

As a Sr Statistical Programmer, you will work closely with biostatisticians to translate statistical analysis plans into efficient programming code, often using SAS or R. You’ll also regularly interact with clinical data managers and project teams to clarify data requirements, resolve data discrepancies, and ensure the accuracy of deliverables. Effective communication and proactive problem-solving are key, as you may be responsible for leading programming efforts, mentoring junior programmers, and ensuring that all outputs meet regulatory and project timelines. This collaborative environment helps ensure the integrity and reproducibility of clinical trial results.

What are the key skills and qualifications needed to thrive as a Sr Statistical Programmer, and why are they important?

To thrive as a Sr Statistical Programmer, you need strong expertise in statistical programming languages like SAS or R, experience with clinical trial data, and a relevant degree in statistics, mathematics, or a related field. Proficiency with CDISC standards (SDTM, ADaM), data management systems, and regulatory submission tools is typically required. Excellent problem-solving, attention to detail, and effective communication are crucial soft skills for collaborating with cross-functional teams and ensuring high data quality. These skills and qualifications are essential for accurate analyses, regulatory compliance, and successful delivery of clinical research projects.
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Sr Statistical Programmer jobs near you
Infographic showing various Sr Statistical Programmer job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 97% Full Time, and 2% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% 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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