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Clinical Statistical Programmer Jobs (NOW HIRING)

LivaNova

Statistical Programmer II

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables, listings, and figures (TLFs) per Statistical Analysis Plans (SAPs) to support new products and ...

New

LivaNova

Statistical Programmer II

Austin, TX

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables, listings, and figures (TLFs) per Statistical Analysis Plans (SAPs) to support new products and ...

LivaNova

Statistical Programmer II

Minneapolis, MN

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables, listings, and figures (TLFs) per Statistical Analysis Plans (SAPs) to support new products and ...

LivaNova

Statistical Programmer II

Houston, TX

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables, listings, and figures (TLFs) per Statistical Analysis Plans (SAPs) to support new products and ...

LivaNova

Statistical Programmer II

Phoenix, AZ

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables, listings, and figures (TLFs) per Statistical Analysis Plans (SAPs) to support new products and ...

LivaNova

Statistical Programmer II

Boston, MA

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables, listings, and figures (TLFs) per Statistical Analysis Plans (SAPs) to support new products and ...

LivaNova

Statistical Programmer II

Atlanta, GA

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables, listings, and figures (TLFs) per Statistical Analysis Plans (SAPs) to support new products and ...

LivaNova, PLC

Statistical Programmer II

Atlanta, GA · On-site

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables, listings, and figures (TLFs) per Statistical Analysis Plans (SAPs) to support new products and ...

LivaNova

Statistical Programmer II

Dallas, TX

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables, listings, and figures (TLFs) per Statistical Analysis Plans (SAPs) to support new products and ...

LivaNova

Statistical Programmer II

Raleigh, NC

$90K - $100K/yr

The statistical programming team develops datasets from our clinical trials and delivers tables, listings, and figures (TLFs) per Statistical Analysis Plans (SAPs) to support new products and ...

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Clinical Statistical Programmer information

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How much do clinical statistical programmer jobs pay per hour?

As of Jun 26, 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 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.

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 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).

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Clinical Statistical Programmer jobs near you
Infographic showing various Clinical Statistical Programmer job openings in the United States as of June 2026, with employment types broken down into 2% Internship, 77% Full Time, 5% Part Time, and 16% Contract. Highlights an 81% In-person, and 19% Remote job distribution, with an average salary of $112,695 per year, or $54.2 per hour.
Clinical Statistical Programmer

Clinical Statistical Programmer

Katalyst HealthCares & Life Sciences

Princeton, NJ • On-site

Other

Posted 29 days ago

Job description

Job Title

Responsibilities:

  • Generate and validate TLFs based on the Statistical Analysis Plan, TLF specifications, and industry best practices.
  • With minimal oversight, perform all programming activities and documentation for assigned studies.
  • Follow departmental Standard Operating Procedures (SOPs) and industry guidance to ensure traceability and regulatory compliance.
  • Support the preparation and review of the electronic regulatory submission.
  • Ensure that all deliverables are completed on time and of high quality.
  • Represent the Clinical Programming function at cross-functional meetings.
  • May support EDC development and visualization tools (PowerBI).

Requirements:

  • Minimum 3-5 years in a clinical programming role.
  • Bachelor's Degree (Data Science, Computer Science, Statistics, Bioinformatics, or related discipline).
  • Independently develop SAS/R programs to generate and validate datasets according to the Statistical Analysis Plan, TLF specifications, and industry best practices.
  • Experience generating outputs for regulatory submissions (FDA) MUST.
  • Programming experience in SQL, JSON (Good to have).
  • Working experience with relational databases. (EDC system, IBM (Zelta).
  • Experience implementing CDISC standards is desirable.
  • Knowledge of EDC development and visualization tools (PowerBI, Tableau) is an asset.
  • Excellent Communications skills, both oral and written.
  • Analytical skills, creativity and innovative approach to problem solving.
  • Propensity for continuous learning and experimentation.
  • Demonstrated initiative and problem-solving skills, critical thinking skills.
Katalyst Healthcares & Life Sciences logo

About Katalyst Healthcares & Life Sciences

Sourced by ZipRecruiter

Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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