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Clinical Programmer Jobs (NOW HIRING)

Clinical SAS Developer

North Wales, PA ยท On-site

$43 - $48/hr

Extensive programming experience in a clinical trial environment (CRO/Pharma). * Expertise in SAS/BASE, SAS/STAT, and SAS/MACRO. * In-depth knowledge of CDISC standards and regulatory submission ...

Clinical SAS Developer

Upper Gwynedd, PA ยท On-site

$43 - $48/hr

Extensive programming experience in a clinical trial environment (CRO/Pharma). * Expertise in SAS/BASE, SAS/STAT, and SAS/MACRO. * In-depth knowledge of CDISC standards and regulatory submission ...

1.Must have 6+ yrs of exp in clinical domain 2.Strong knowledge of SDTM 3.Create advanced SAS ... Act as the primary programming point of contact for biostatisticians and study teams 5.Perform peer ...

Clinical Engineer - Hybrid

Lebanon, NH ยท On-site

$42.31 - $67.70/hr

Achieves clinical engineering operational objectives by contributing clinical engineering information and recommendations to strategic plans and reviews; preparing and completing action plans ...

$41.14 - $61.20/hr

Job Summary and Responsibilities As a Clinical Engineering Project Engineer, you will manage the planning and implementation of key projects for Clinical Engineering by developing plans, identifying ...

Admin Director- Clinical Engineering

Springfield, MO ยท On-site

$91K - $117K/yr

Benefits | CoxHealth The Administrative Director, Clinical Engineering provides strategic and operational leadership for biomedical services, clinical engineering, medical equipment support, and ...

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Clinical Programmer information

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How much do clinical programmer jobs pay per hour?

As of Jun 26, 2026, the average hourly pay for clinical programmer in the United States is $64.77, according to ZipRecruiter salary data. Most workers in this role earn between $53.61 and $73.32 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Programmer, and why are they important?

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 are clinical programmers and what do they do?

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.

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.

More about Clinical Programmer jobs
What cities are hiring for Clinical Programmer jobs? Cities with the most Clinical Programmer job openings:
What states have the most Clinical Programmer jobs? States with the most job openings for Clinical Programmer jobs include:
What job categories do people searching Clinical Programmer jobs look for? The top searched job categories for Clinical Programmer jobs are:
Infographic showing various Clinical Programmer job openings in the United States as of June 2026, with employment types broken down into 33% Full Time, and 67% Contract. Highlights an 100% In-person job distribution, with an average salary of $134,731 per year, or $64.8 per hour.
Clinical SAS Developer

Clinical SAS Developer

Cynet Systems

North Wales, PA โ€ข On-site

$43 - $48/hr

Other

Posted 3 days ago


Job description

Job Overview

Pay Range: $43hr - $48hr

Requirement/Must Have:
  • 6-8 years of experience in the clinical domain.
  • Strong knowledge of SDTM.
  • Extensive programming experience in a clinical trial environment (CRO/Pharma).
  • Expertise in SAS/BASE, SAS/STAT, and SAS/MACRO.
  • In-depth knowledge of CDISC standards and regulatory submission requirements.
Responsibilities:
  • Create advanced SAS macros, templates, and utilities for efficient data processing.
  • Act as the primary programming point of contact for biostatisticians and study teams.
  • Perform peer review of code and documentation for accuracy and traceability.
  • Review CRF (Case Report Form) annotations and data specifications.
  • Ensure compliance with CDISC standards (SDTM/ADaM) and FDA/ICH guidelines.

Cynet Systems logo

About Cynet Systems

Sourced by ZipRecruiter

Cynet Systems Inc is a staffing and recruiting corporation nestled in Ashburn, VA, USA. Established in 2010, the company operates within the Information Technology and Services sector, specializing in providing effective workforce solutions to different business needs, including IT consulting, direct hire, and contract staffing services. Through the years, Cynet Systems has built an impressive portfolio, going beyond borders and expanding its operations internationally in Canada and India. Rooted in its core values of teamwork, leadership, and commitment, Cynet Systems helps businesses unlock their full potential by providing versatile and competent professionals that perfectly align with their needs. Fueled by their unwavering mission to deliver top-tier talent to businesses worldwide, Cynet Systems garnered various recognitions including SIA's fastest-growing staffing firms and Best Place to Work in Virginia for 2019.

Industry

It services

Company size

501 - 1,000 Employees

Headquarters location

Sterling, VA, US

Year founded

2010

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