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Clinical Statistical Programmer Jobs (NOW HIRING)

Intego Group

NY · On-site

$90 - $120/hr

Senior/Principal Clinical Statistical Programmer USA Intego Clinical's office in Florida, USA, is looking for experienced Senior/Principal Clinical Statistical Programmers to join our global team ...

LivaNova

Statistical Programmer II

Austin, TX · On-site

$90K - $100K/yr

Accountable for clinical statistical programming deliverables and for ensuring excellence in programming activities in terms of quality and timelines for clinical trials under the responsibility of ...

LivaNova

Statistical Programmer II

Atlanta, GA · On-site

$90K - $100K/yr

Accountable for clinical statistical programming deliverables and for ensuring excellence in programming activities in terms of quality and timelines for clinical trials under the responsibility of ...

LivaNova

Statistical Programmer II

Boston, MA · On-site

$90K - $100K/yr

Accountable for clinical statistical programming deliverables and for ensuring excellence in programming activities in terms of quality and timelines for clinical trials under the responsibility of ...

LivaNova

Statistical Programmer II

Phoenix, AZ · On-site

$90K - $100K/yr

Accountable for clinical statistical programming deliverables and for ensuring excellence in programming activities in terms of quality and timelines for clinical trials under the responsibility of ...

LivaNova

Statistical Programmer II

$90K - $100K/yr

Accountable for clinical statistical programming deliverables and for ensuring excellence in programming activities in terms of quality and timelines for clinical trials under the responsibility of ...

LivaNova

Statistical Programmer II

Raleigh, NC · On-site

$90K - $100K/yr

Accountable for clinical statistical programming deliverables and for ensuring excellence in programming activities in terms of quality and timelines for clinical trials under the responsibility of ...

LivaNova

Statistical Programmer II

Minneapolis, MN · On-site

$90K - $100K/yr

Accountable for clinical statistical programming deliverables and for ensuring excellence in programming activities in terms of quality and timelines for clinical trials under the responsibility of ...

LivaNova

Statistical Programmer II

Houston, TX · On-site

$90K - $100K/yr

Accountable for clinical statistical programming deliverables and for ensuring excellence in programming activities in terms of quality and timelines for clinical trials under the responsibility of ...

LivaNova

Statistical Programmer II

Dallas, TX · On-site

$90K - $100K/yr

Accountable for clinical statistical programming deliverables and for ensuring excellence in programming activities in terms of quality and timelines for clinical trials under the responsibility of ...

SystImmune, Inc

Statistical Programmer

Redmond, WA · On-site

$80K - $100K/yr

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond ... The Statistical Programmer will support statistical programming activities for clinical trials ...

Rhythm Pharmaceuticals

Statistical Programmer

Boston, MA · On-site

$110K - $165K/yr

This role will provide statistical programming hands-on support across clinical studies, regulatory submissions, and cross-functional development activities. The successful candidate will be ...

Systimmune

Statistical Programmer

Redmond, WA · On-site

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond ... The Statistical Programmer will support statistical programming activities for clinical trials ...

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Clinical Statistical Programmer information

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How much do clinical statistical programmer jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for clinical statistical programmer in the United States is $54.18, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $81.49 per hour, depending on experience, location, and employer.

What does a clinical statistical programmer do?

A Clinical Statistical Programmer is responsible for managing and analyzing clinical trial data using statistical software, such as SAS or R. Their primary tasks include creating datasets, programming statistical analyses, and generating tables, listings, and figures for clinical study reports. They work closely with biostatisticians and clinical research teams to ensure data accuracy and regulatory compliance. Their work is essential for supporting submissions to regulatory agencies and for making data-driven decisions in clinical research.

What does a clinical statistical programmer do?

The job duties of a clinical statistical programmer involve collecting data, performing statistical analysis, and analyzing data sets according to the needs of their employer or client. Your responsibilities in this career may involve using SAS programming to create and analyze data sets during clinical trials or other clinical experiments and studies. You may also be involved in performing data integration for reports following clinical research or statistical analysis for quality control (QC).

What are the key skills and qualifications needed to thrive as a clinical statistical programmer, and why are they important?

To thrive as a Clinical Statistical Programmer, you need strong proficiency in statistical programming languages (such as SAS or R), a background in statistics or life sciences, and familiarity with clinical trial processes. Experience with CDISC standards (SDTM, ADaM), regulatory submission requirements, and version control systems is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for collaborating with cross-functional teams and ensuring data quality. These skills ensure the accurate analysis and reporting of clinical data, which is critical for regulatory compliance and successful clinical trial outcomes.

What are some common challenges faced by clinical statistical programmers when working with clinical trial data?

Clinical Statistical Programmers often encounter challenges such as handling large and complex datasets, ensuring data integrity, and adhering to strict regulatory guidelines (like CDISC standards). Collaborating closely with biostatisticians, data managers, and clinical teams is essential to resolve data discrepancies and meet tight project deadlines. Staying updated on evolving regulatory requirements and software tools is also vital to maintain high-quality deliverables in a fast-paced environment.
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Clinical Statistical Programmer jobs near you
Infographic showing various Clinical Statistical Programmer job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $112,695 per year, or $54.2 per hour.

Senior/Principal Clinical Statistical Programmer

Intego Group

NY • On-site

$90 - $120/hr

Other

Posted 8 days ago

Job description

Senior/Principal Clinical Statistical Programmer

USA

Intego Clinical’s office in Florida, USA, is looking for experienced Senior/Principal Clinical Statistical Programmers to join our global team working from the office or remotely.

As a clinical project team member, the Senior/Principal Clinical Statistical Programmer applies advanced‑level programming techniques and leadership to the planning, design, development, implementation, and maintenance of software for the monitoring, reporting, and analysis of clinical trials.

Job responsibilities:

The Senior/Principal Clinical Statistical Programmer will be responsible for overall timelines and significant project milestones, and overall project quality, integrity, and productivity. May serve on or lead a departmental initiative, specialized projects, and working groups. Can serve as a project team leader. This senior position should be capable of developing and maintaining software development tools and standard templates. Also, this person should be a Subject Matter Expert (SME) as a technology troubleshooter.

  • Responsible for the processing of clinical data required for analysis of clinical trials for Phase 1‑4.
  • Develop SAS coding and table templates for preparing, processing, and analyzing clinical data.
  • Generate and QC summary tables, data listings, and graphs for in‑house analyses of study data or publications using SAS standard coding practices.
  • Create/acquire tools to improve programming efficiency or quality.
  • Validate the work of other programmers/analysts.
  • Create/review programming plan, specifications for datasets, and TLF’s.
  • Establish monitoring of data transfers for ongoing trials to identify study conduct or data quality issues.
  • Support data queries from other functional groups (Biostatistics, Medical Writing, Clinical Development, Clinical Operations, Regulatory, and Marketing).
General requirements:
  • A minimum of a Bachelor’s degree in Computer Science, Mathematics, Statistics, Pharmaceuticals Sciences, Life Sciences, and related areas is required. A Master’s is preferred.
  • A minimum of 4 years of hands‑on relevant career experience in the pharmaceutical or biotechnology industry.
  • Have excellent knowledge of SAS programming and associated features and their applications in the pharmaceuticals industry environment, particularly clinical trial data sets.
  • Familiar with CDISC conventions, i.e., SDTM and ADaM models, and hands‑on experience implementing these models.
  • Strong understanding of clinical trial data and hands‑on in data manipulations, analysis, and reporting of analysis results.
  • Must understand the role of all the functional areas in the clinical trial process.
  • Must have a basic understanding of the FDA/ICH guidelines, the software development life cycle, 21 CFR Part 11, and other relevant FDA regulations.
  • Must possess the knowledge and application of p‑values, confidence intervals, linear regression analysis, advanced general linear models, frequencies, survival analysis, non‑parametric analysis, randomization software, and demonstrate proficiency in implementing new ideas in clear, efficient SAS code for the purposes of data analysis and reporting.
  • Must demonstrate intermediate UNIX, Oracle Clinical or equivalent clinical DM system, and relational database theory.
  • Track record of generating new ideas and solutions to data analysis.
  • Thorough understanding of relational database components and theory.
  • SAS certification is an advantage.
  • It would be an asset to have had experience working on FDA submissions.
  • The candidate should demonstrate clear and timely written and verbal communication with peers, customers, and management.
  • Should be able to present effective presentations to small groups such as Project Teams or during Statistical Programming meetings.
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