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Clinical Programmer Jobs (NOW HIRING)

Tandym Tech

Clinical Programmer

Woburn, MA · On-site

A Massachusetts-based pharma company is actively seeking a new Clinical Programmer to join its team. The role offers a dynamic work environment with opportunities for innovation in the healthcare ...

CTI

Clinical Programmer

Covington, KY · On-site +1

A Clinical Programmer will support the design, development, and validation of clinical trial databases. In this role, you will build and test study databases using platforms such as Medidata Rave or ...

Cytel

Senior Clinical Programmer

Cambridge, MA · On-site +1

We are seeking an experienced and skilled Clinical Programmer with a strong background within clinical programming. The ideal candidate will have 4-6 years of experience in clinical data programming ...

CTI

Clinical Programmer

Covington, KY · On-site +1

A Clinical Programmer will support the design, development, and validation of clinical trial databases. In this role, you will build and test study databases using platforms such as Medidata Rave or ...

Recor Medical

Senior Clinical Programmer

Palo Alto, CA · On-site

$145K - $156K/yr

Position Summary The Senior Clinical Programmer at ReCor Medical requires complete knowledge and full understanding of clinical programming principles and practices for medical device clinical trials.

Lilly

OR

The Clinical Study Build Programmer - eCOA is responsible for programming and testing clinical trial data collection databases, including the mapping, testing and normalization of data into a ...

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How much do clinical programmer jobs pay per hour?

As of Jun 4, 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.

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 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.

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.

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Clinical Programmer jobs near you
Infographic showing various Clinical Programmer job openings in the United States as of May 2026, with employment types broken down into 1% Locum Tenens, 3% As Needed, 78% Full Time, and 18% Part Time. Highlights an 90% Physical, 4% Hybrid, and 6% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.

Clinical Programmer

Tandym Tech

Woburn, MA • On-site

Other

This job post has expired 1 day ago. Applications are no longer accepted.

Job description



A Massachusetts-based pharma company is actively seeking a new Clinical Programmer to join its team. The role offers a dynamic work environment with opportunities for innovation in the healthcare industry.


Responsibilities:



  • Developing and validating SAS programs to generate data review, cleaning, and reconciliation listings

  • Programming listings, tables, profiles, figures, and datasets according to specifications

  • Debugging and improving existing SAS programs and macros

  • Administering user management in EDC systems

  • Creating SAS macros/SQL to enhance programming efficiency

  • Performing other duties, as needed


Qualifications:



  • 2+ years of proven experience in Pharma/Biotech/SAS Programming

  • Bachelor's degree or higher in a Scientific, Biological, Statistical, and/or Computer Science field

  • SAS Certification

  • Analytical and problem-solving skills

  • Interpersonal and communication skills

  • Organizational and time-management skills


Desired Qualifications:



  • Master's Degree in Stats/Math/Epidemiology degree

  • Familiarity with industry standards such as CDISC/CDASH

  • SAS programming projects experience


Apply