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Clinical Statistical Programmer Jobs in Connecticut

micro1 AI

Director of Biostatistics

Stamford, CT · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

micro1 AI

Director of Biostatistics

New Haven, CT · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

micro1 AI

Director of Biostatistics

Hartford, CT · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

micro1 AI

Director of Biostatistics

Bridgeport, CT · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

micro1 AI

Director of Biostatistics

Waterbury, CT · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a dynamic customer project focused on AI-assisted clinical research. In this role, you'll apply your ...

LanceSoft Inc

Quality Engineer III

North Haven, CT · On-site

$71K - $92K/yr

LanceSoft specializes in recruiting and retaining top clinical research & scientific talent for ... Statistical Quality control/statistical process control, design of experiments, failure mode and ...

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All JobsClinical Statistical Programmer JobsClinical Statistical Programmer Jobs in Connecticut

Clinical Statistical Programmer information

See Connecticut salary details

$15

$51

$85

How much do clinical statistical programmer jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for clinical statistical programmer in Connecticut is $51.54, according to ZipRecruiter salary data. Most workers in this role earn between $32.69 and $77.50 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 Connecticut as of August 2026, with employment types broken down into 3% As Needed, 70% Full Time, 16% Part Time, 2% Temporary, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $107,205 per year, or $51.5 per hour.

Manager, Clinical Programming (Remote)

Penfield Search Partners

Fairfield, CT • On-site, Remote

Full-time

Re-posted 5 days ago

Job description

Job Description Contact: Neisha Camacho/Terra Parsons - teamnt@penfieldsearch.com No 3rd party candidates Position Summary We are seeking an experienced Senior Clinical Programmer to support clinical development programs by delivering high-quality programming solutions for medical monitoring, data management, and statistical programming activities. The ideal candidate has strong expertise in CDISC standards, SDTM dataset development, and modern programming tools including SAS and R. This role partners closely with cross-functional teams to develop efficient, compliant, and scalable programming solutions that support ongoing clinical trials

Key Responsibilities Provide programming support for medical monitoring, data management, and statistical programming activities across clinical studies. Develop specifications for SDTM dataset creation in accordance with CDISC SDTM Implementation Guide (SDTM IG). Program, validate, and maintain CDISC-compliant SDTM datasets.

Create and maintain annotated CRFs (aCRFs) aligned with SDTM specifications. Generate outputs and listings to support medical monitoring, data review, statistical endpoint monitoring, and data management activities. Develop, enhance, and maintain SAS macros, R functions, and other reusable programming utilities.

Design, develop, test, and implement programming solutions to address complex business and study requirements. Ensure programming deliverables meet quality standards, timelines, and regulatory expectations. Collaborate effectively with cross-functional teams including Biostatistics, Data Management, Clinical Operations, and Medical Monitoring.

Manage multiple projects simultaneously while delivering high-quality work within established timelines. Qualifications Bachelor's degree in Statistics, Computer Science, Mathematics, Life Sciences, or a related discipline (or equivalent experience). Experience programming in the pharmaceutical, biotechnology, or related regulated industry preferred.

Advanced programming proficiency in SAS, R, and SQL. Strong working knowledge of CDISC standards, including SDTM and annotated CRFs. Experience with JReview is highly preferred.

Experience with Shiny, Pharmaverse, and R Markdown is preferred. Familiarity with programming languages such as Python, VBA, or C++ is a plus. Excellent analytical, problem-solving, and communication skills.

Ability to work independently while collaborating effectively within cross-functional teams. Strong organizational skills with the ability to prioritize multiple assignments and meet deadlines. Preferred Experience Experience supporting medical review or clinical data review activities.

Experience developing reusable programming utilities and automation tools. Familiarity with regulatory submission standards and clinical trial data workflows. Experience working in a fast-paced clinical development environment.

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