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Senior Statistical Programmer Analyst Jobs (NOW HIRING)

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 ...

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 ...

Rho

Senior Statistical Programmer

Durham, NC · On-site

Whether you're a data wizard, analytical genius, project mastermind, or any other role, you'll fit ... As a Senior Statistical Programmer, you'll have the opportunity to design and write program ...

Rho Inc

Senior Statistical Programmer

Whether you're a data wizard, analytical genius, project mastermind, or any other role, you'll fit ... As a Senior Statistical Programmer, you'll have the opportunity to design and write program ...

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How much do senior statistical programmer analyst jobs pay per year?

As of Jul 1, 2026, the average yearly pay for senior statistical programmer analyst 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 the key skills and qualifications needed to thrive as a Senior Statistical Programmer Analyst, and why are they important?

To thrive as a Senior Statistical Programmer Analyst, you need advanced programming skills in SAS or R, a strong background in statistics, and a relevant degree such as in mathematics, statistics, or computer science. Experience with clinical trial data, CDISC standards (SDTM, ADaM), and regulatory submission processes, along with certifications like SAS Certified Professional, are highly valued. Exceptional problem-solving abilities, attention to detail, and effective communication enable you to manage complex datasets and collaborate with cross-functional teams. These combined skills ensure accurate data analysis, regulatory compliance, and successful delivery of biostatistical projects in the pharmaceutical or clinical research industry.

What does a Senior Statistical Programmer Analyst do?

A Senior Statistical Programmer Analyst is responsible for designing, developing, and validating statistical programs that analyze clinical trial or research data. They work closely with biostatisticians and data managers to ensure data accuracy, integrity, and compliance with regulatory standards. Their work includes creating tables, listings, and figures (TLFs), developing analysis datasets, and automating data processes. Senior Statistical Programmer Analysts often mentor junior programmers and play a key role in quality control and project delivery within pharmaceutical, biotechnology, or clinical research organizations.

How does a Senior Statistical Programmer Analyst typically collaborate with cross-functional teams in clinical research projects?

As a Senior Statistical Programmer Analyst, you will regularly collaborate with biostatisticians, data managers, clinical research associates, and project managers. Your main responsibility is to translate statistical analysis plans into programming code (often using SAS or R), ensuring datasets and outputs meet regulatory standards. You’ll participate in team meetings to clarify study requirements, address data or programming issues, and ensure timelines are met. Strong communication and documentation skills are essential, as you often serve as a bridge between technical and non-technical team members.
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Senior Statistical Programmer

Senior Statistical Programmer

Navitas Life Sciences

Remote

Full-time

Posted 25 days ago

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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