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Sr Statistical Programmer Jobs (NOW HIRING)

The Senior Statistical Programmer Analyst I (SR SPA I) is an independent statistical programmer analyst supporting the clinical reporting production programming and verification for client regulatory ...

Senior Statistical Programmer

Irvine, CA · On-site

$75 - $98.48/hr

Title: Senior Statistical Programmer Dura tion: Jun 8 Dec 31, 2026 Location: Irvine, CA, 92618 Schedule: 1st Shift, 9: 00 AM - 5: 00 PM TECHNICAL SKILLS Must Have * Base SAS * Clinical Data ...

Edetek is seeking a highly skilled Senior Statistical Programmer to join our dynamic team. As a leader in data analytics, we are dedicated to providing innovative solutions to our clients in the ...

Position Summary A Senior Statistical Programming is an expert in the management, technical oversight, and quality of statistical programming activities related to the analyses of clinical trial data ...

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Sr Statistical Programmer information

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$82.5K

$128.3K

$167.5K

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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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.
Sr. Statistical Programmer

Other

Posted 15 days ago


Job description

SUMMARY:

A biopharmaceutical company in the Bay area needs a very strong Senior Statistical Programmer to support their team. This programmer will need to be a strong, senior-level programmer who can work well both independently and part of a team. They must be proficient in their CDISC expertise and be able to program specifications from scratch (both SDTM and ADaM programming).


DUTIES & RESPONSIBILITIES:

  • Perform data manipulation, analysis and reporting of clinical trial data
  • Program and generate tables, listings, and graphs (TLGs)
  • Participate in the review of statistical analysis plans, table specification, develop specification for SDTM and ADaM data sets.
  • Review, and comment on CRFs, annotated CRFs, and edit checks and related documents.
  • Participate in study team meetings and address issues that may affect statistical programming.
  • Validate and document SAS programs and output
  • Create SDTM and ADaM Datasets and related documentation
  • Fulfill ad-hoc programming requests
  • Other duties as needed


QUALIFICATIONS & REQUIREMENTS:

  • 15+ years of statistical programming experience in the pharmaceutical/biotech industries, good tenure with Sponsor companies
  • Strong submissions experience (BLA, NDA/sNDA and EMA), understanding submission requirements, and end to end programming experience
  • Strong experience with CDISC implementation – SDTM/ADAM, must be able to develop specifications from scratch
  • Demonstrated ability performing all levels of programming activities for a clinical project
  • Experience working in the Cardiovascular or Neuromuscular areas is a plus