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Navitas Life Sciences

Senior Statistical Programmer

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 ...

Solomon Page

Sr. Statistical Programmer

Princeton, NJ · On-site

$75 - $80/hr

The Senior Statistical Programmer plays a critical role in supporting clinical development programs by providing expert statistical programming leadership across ongoing studies, regulatory ...

ImmunityBio

Senior Statistical Programmer

Dunkirk, NY · On-site

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 ...

EDETEK

Senior Statistical Programmer

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 ...

Cytel

Senior Statistical Programmer FSP

Cambridge, MA · On-site +1

As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are ...

Syneoshealth

Sr Statistical Programmer (NA Only)

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 Sep 2, 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 is a Sr Statistical Programmer?

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.

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

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.

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.
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Sr Statistical Programmer jobs near you
Infographic showing various Sr Statistical Programmer job openings in the United States as of August 2026, with employment types broken down into 77% Full Time, 8% Part Time, and 15% Contract. Highlights an 62% In-person, and 38% Remote job distribution, with an average salary of $128,293 per year, or $61.7 per hour.

Senior Statistical Programmer

Navitas Life Sciences

Remote

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Job Description
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 submissions and publications.
Critical client project activities are reporting database development (SDTM and ADaM), statistical and clinical reporting, verification and submissions support.
About the Role
  • Independently, perform SAS programming and analysis support of the generation of analysis datasets, statistical analysis, listings, figures and tables;
  • Independently, develop SAS application code;
  • Independently, perform validation of SAS programs and deliverables;
  • Independently, perform migrations and verifications;
  • Independently, perform SDTM and ADaM mapping;
  • Generate SDTM and ADaM deliverables;
  • Generate all necessary output for the compilation of statistical appendices for CTR, ISS, and ISE;
  • Generate data files and/or output for safety updates, publications and meeting presentations;
  • Interface with a cross-function of client and DataCeutics team members; and
  • Act as an Expert in one or more areas that may include Project Management, SCE, SDTM, ADaM, define.xml, SAS programming, deliverables process, Tables, Graphics, PK/PD, Registries or other areas.

Desirable Skills and Experience
  • Background in statistics and statistical analysis is desirable
  • 10 plus years Pharmaceutical or CRO industry experience in clinical reporting and statistical programming
  • Strong competence in SAS/Base, SAS/Macro, and SAS/STAT programming
  • Working knowledge of CDISC, SDTM and ADaM
  • Expert knowledge of SAS-based statistical programming
  • Proficiency in SAS programming on multiple platforms and operating systems, e.g. Windows, UNIX, etc. is desirable

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