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Clinical Programmer Jobs (NOW HIRING)

Immunome, Inc.

SeniorEDC Programmer

Bothell, WA · On-site

This role will work closely with Clinical Data Management, Biostatistics, Clinical Operations, and ... Oversee and/or mentor junior programmers or external vendors. * Contribute to SOP development and ...

Systimmune

EDC Programmer

Redmond, WA · On-site

$100K - $150K/yr

Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer ... The EDC Programmer (EDCP) is a critical technical role responsible for building, configuring, and ...

SystImmune, Inc

EDC Programmer

Redmond, WA · On-site

$100K - $150K/yr

Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer ... The EDC Programmer (EDCP) is a critical technical role responsible for building, configuring, and ...

Atorus Research

Sr Medidata RAVE Programmer

S. or Canada Contract/Corp to Corp JOB OVERVIEW The Electronic Data Capture (EDC) Programmer is responsible for providing support in creating, deploying and maintaining clinical databases and ...

Berkshire Health Systems

Clinical Analyst

Pittsfield, MA · On-site

$36.08/hr

In conjunction with the clinical programmer(s) or vendors, this position will assist in problem determination, system design, program testing, and performing Quality Control checks on programs and ...

Berkshire Health Systems

Clinical Analyst

Pittsfield, MA · On-site

$36.08/hr

In conjunction with the clinical programmer(s) or vendors, this position will assist in problem determination, system design, program testing, and performing Quality Control checks on programs and ...

HCL America Inc.

Clinical SAS SDTM

North Wales, PA

Act as the primary programming point of contact for biostatisticians and study teams * Perform peer ... Extensive programming experience in a clinical trial environment (CRO/Pharma). * Expertise in SAS ...

D-H Lebanon-MHMH

Clinical Engineer - Hybrid

Lebanon, NH · 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 ...

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Clinical Programmer information

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$24

$64

$102

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.

More about Clinical Programmer jobs
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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.
SeniorEDC Programmer

SeniorEDC Programmer

Immunome, Inc.

Bothell, WA • On-site

Other

Posted 27 days ago

Job description

Position Overview

The Senior EDC (Electronic Data Capture) Programmer (Sr. EDCP) is responsible for leading the design, development, and maintenance of clinical trial databases in an EDC system. This role will work closely with Clinical Data Management, Biostatistics, Clinical Operations, and external vendors to ensure high-quality, compliant data collection systems that support efficient trial execution. 

Responsibilities

  • Lead the design, build, validation, and deployment of a study build within an EDC system. 
  • Develop and maintain edit checks, custom functions, derivations, and integrations. 
  • Review study protocols and provide input on CRF design and database structure. 
  • Collaborate with Data Management to ensure alignment with data standards (CDISC, SDTM where applicable). 
  • Perform User Acceptance Testing (UAT) and support database releases and migrations. 
  • Ensure EDC systems comply with regulatory requirements (FDA, ICH-GCP, 21 CFR Part 11). 
  • Troubleshoot and resolve database issues in a timely manner. 
  • Oversee and/or mentor junior programmers or external vendors. 
  • Contribute to SOP development and process improvements. 
  • Support data integrations with external systems (IRT, ePRO, labs, etc.). 
  • Maintain documentation including specifications, validation records, and audit trails. 

Qualifications

  • Bachelor's degree in relevant field. 
  • A minimum of 5 years of EDC programming experience in the biotech/pharma industry. Oncology experience is preferred.  

Knowledge and Skills

  • Strong hands-on experience with at least one major EDC platform (Medidata Rave preferred). 
  • Solid understanding of clinical trial processes and data flow. 
  • Experience with CDISC standards (SDTM, CDASH) is preferred. 
  • Familiarity with regulatory requirements (ICH-GCP, 21 CFR Part 11). 
  • Strong problem-solving skills and attention to detail. 
  • Ability to manage multiple studies and priorities. 

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