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Clinical Programmer Jobs in Connecticut (NOW HIRING)

Trimedx

Clinical Engineering IT Technician

Stamford, CT · On-site

$20.25 - $26/hr

Annual Merit Increases Summary Aligned with the TRIMEDX Vision, Mission and Values, the primary role of a Clinical Engineering - IT Technician is to support the operations of the Clinical Engineering ...

Yale New Haven Health

Clinical Engineer

New Haven, CT · On-site

Experience in leading the planning, design, implementation and support of clinical engineering integrations. Facilitates the enterprise wide collaboration of multiple departments necessary to support ...

Yale New Haven Health

Clinical Engineer

New Haven, CT · On-site

Experience in leading the planning, design, implementation and support of clinical engineering integrations. Facilitates the enterprise wide collaboration of multiple departments necessary to support ...

Yale New Haven Health

Clinical Engineer

New Haven, CT · On-site

Experience in leading the planning, design, implementation and support of clinical engineering integrations. Facilitates the enterprise wide collaboration of multiple departments necessary to support ...

Trinity Health

THCE Clinical Engineering Manager

Hartford, CT · On-site

$100K - $130K/yr

POSITION PURPOSE Responsible for day-to-day operations of the Unified Enterprise Ministry's (UEM) Trinity Health Clinical Engineering (THCE) program at Regional Health Ministry (RHM) Hospital and ...

Trimedx

Biomedical Engineering Intern

Stamford, CT · On-site

$17.75 - $23.25/hr

Summary The TRIMEDX Biomedical Engineering Intern gains on the job training by shadowing experienced clinical engineers, biomedical engineers, lab engineers, and radiology engineers under the close ...

TRIMEDX Holdings

Biomedical Engineering Intern

Stamford, CT

$17.75 - $23.25/hr

Summary The TRIMEDX Biomedical Engineering Intern gainson the job training by shadowing experienced clinical engineers, biomedical engineers, lab engineers, and radiology engineers under the close ...

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All JobsClinical Programmer JobsClinical Programmer Jobs in Connecticut

Clinical Programmer information

See Connecticut salary details

$23

$61

$97

How much do clinical programmer jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for clinical programmer in Connecticut is $61.62, according to ZipRecruiter salary data. Most workers in this role earn between $51.01 and $69.76 per hour, depending on experience, location, and employer.

How do you become a clinical programmer?

To become a clinical programmer, typically a bachelor's degree in computer science, health informatics, or a related field is required. Gaining experience with programming languages such as SAS, SQL, or R, and understanding clinical trial processes and regulatory requirements are important. Certifications like the SAS Certified Clinical Trials Programmer can also enhance job prospects.

What are the key skills and qualifications needed to thrive as a clinical programmer?

To thrive as a Clinical Programmer, you need strong proficiency in programming languages like SAS or R, a solid understanding of clinical trial processes, and typically a degree in life sciences, computer science, or a related field. Expertise with clinical data management systems (CDMS), electronic data capture (EDC) tools, and CDISC standards such as SDTM and ADaM is often required. Attention to detail, problem-solving ability, and effective communication are vital soft skills for ensuring data accuracy and collaborating with cross-functional teams. Mastery of these skills ensures the integrity and reliability of clinical trial data, supporting regulatory compliance and successful study outcomes.

What is a clinical programmer?

Clinical programmers are professionals who design, develop, and maintain computer programs used to manage and analyze clinical trial data in the pharmaceutical and biotech industries. They work closely with data managers, statisticians, and clinical teams to ensure data accuracy and regulatory compliance. Their responsibilities often include writing programs for data cleaning, statistical analysis, and generating reports using tools like SAS or R. Clinical programmers play a key role in ensuring that clinical trial data is processed efficiently and meets industry standards.

What do clinical programmers do?

Clinical programmers develop and maintain software programs that support clinical trials, such as data collection, management, and analysis tools. They use programming languages like SAS or R and work closely with data managers and statisticians to ensure accurate and compliant trial data processing.

How does a clinical programmer typically collaborate with biostatisticians and data managers during a clinical trial?

Clinical Programmers work closely with biostatisticians and data managers throughout the clinical trial process. They are responsible for programming data listings, tables, and figures based on statistical analysis plans provided by biostatisticians. Collaboration involves ensuring data integrity, resolving data discrepancies, and implementing database validation checks, often through regular meetings and shared documentation. This teamwork is essential for maintaining data quality and meeting regulatory requirements, making strong communication and coordination skills important in the role.

What is the difference between Clinical Programmer vs Data Manager?

AspectClinical ProgrammerData Manager
Required CredentialsBachelor's degree in life sciences, computer science, or related field; programming skills in SAS, R, or SQLBachelor's degree in health sciences, statistics, or related field; experience with data management software
Work EnvironmentCollaborates with statisticians, data managers, and clinical teams to develop and validate data reportsOversees data collection, validation, and database management for clinical trials
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, clinical research organizations

While both Clinical Programmers and Data Managers work within clinical research, Clinical Programmers primarily focus on developing data reports and programming analysis datasets, whereas Data Managers handle data collection, validation, and database management. Both roles require strong analytical skills and familiarity with clinical data standards, often working closely together to ensure data quality and integrity in clinical trials.

What are popular job titles related to Clinical Programmer jobs in Connecticut? For Clinical Programmer jobs in Connecticut, the most frequently searched job titles are:
What job categories do people searching Clinical Programmer jobs in Connecticut look for? The top searched job categories for Clinical Programmer jobs in Connecticut are:
What are popular job titles related to Clinical Programmer jobs in CT? For Clinical Programmer jobs in CT, the most frequently searched job titles are:
Clinical Programmer jobs near you
Infographic showing various Clinical Programmer job openings in Connecticut as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $128,168 per year, or $61.6 per hour.

Manager, Clinical Programming (Remote)

Penfield Search Partners

Fairfield, CT • On-site, Remote

Full-time

Posted 21 days ago

Job description

Contact: Neisha Camacho/Terra Parsons -
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.