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Clinical Programmer Jobs (NOW HIRING)

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.

We're looking for a Senior Clinical Programmer I who thrives on solving complex challenges and transforming clinical data into high-quality, reliable insights that drive drug development. In this ...

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 ...

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 ...

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 ...

Celerion is committed to swift, exceptional clinical research through translational medicine. Every ... Programmer . You will be responsible for administration of EDC Database including evaluation ...

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Clinical Programmer information

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How much do clinical programmer jobs pay per hour?

As of Aug 5, 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.

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.

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:
Infographic showing various Clinical Programmer job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.

Senior Clinical Programmer

Recor Medical

Palo Alto, CA

$145K - $156K/yr

Full-time

Re-posted 16 days ago


Job description

At Recor Medical, we are pioneering Ultrasound Renal Denervation (uRDN) therapy to treat hypertension, the leading cardiovascular risk factor in the world. With our Paradise uRDN System, we're on a mission to provide the millions of people who suffer from hypertension with a non-drug and minimally invasive option to lower their blood pressure. Join us on our journey and make a meaningful impact on the lives of people around the globe.

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. Responsible for designing, developing, and maintaining clinical data management systems that support regulatory submissions and ensure data integrity throughout clinical trials. Works independently to solve diverse problems related to clinical data processing, applying sophisticated analytical techniques to identify and resolve complex issues. Collaborates with cross-functional teams while providing technical guidance on clinical data processing methodologies.

Responsibilities and Duties

  • Design and develop custom applications, scripts, and tools for clinical data collection, processing, and analysis

  • Establish and enforce data standardization practices (e.g., CDISC, SDTM, ADaM)

  • Collaborate with cross-functional teams including clinical operations, biostatistics, and regulatory affairs

  • Assess unusual circumstances and use sophisticated analytical techniques to identify and resolve complex data issues

  • Generate reports and visualizations for clinical studies

  • Program, validate, and maintain table listings and figures (TLFs) for clinical study reports and regulatory submissions

  • Create and maintain data integration pipelines between clinical systems and internal databases

  • Provide technical guidance to junior programmers on clinical data processing methodologies

  • Other Duties as assigned.

Requirements

  • Bachelor's degree in computer science, statistics, life sciences, or a related field with a minimum of 5 years of related experience; or Master's degree with 3 years of experience; or equivalent work experience.

  • Proficiency in R, with experience in other relevant programming languages (e.g., Python, SQL, SAS).

  • Comprehensive understanding of clinical trial processes, data flow, and clinical trial data standards (e.g., CDISC SDTM, ADaM).

  • Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams and explain technical concepts to non-technical stakeholders.

  • Knowledge of regulatory requirements and experience preparing programming deliverables for submissions to regulatory agencies.

Preferred Skills

  • Experience with data visualization tools (e.g., Power BI, Tableau)

  • Proficiency in version control systems (e.g., Git) and collaborative development practices

  • Experience mentoring junior programmers and conducting code reviews

  • Familiarity with cloud-based data platforms and integration technologies

  • Experience with software validation per FDA guidelines

  • Knowledge of machine learning or advanced analytics techniques applicable to clinical data

Salary range: $145,604- $156,347 (Annual Base Salary)

The successful candidate's starting base pay will be determined based on job-related skills, experience, qualifications, work location and market conditions. The expected base pay range for this role may be modified based on market conditions.


Equal Employment Opportunity
At Recor Medical, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer, we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.


Pre-Employment Requirements

At Recor Medical, patient safety, integrity, and regulatory compliance are foundational to everything we do. To support these standards,employmentis contingent upon meeting the following requirements:


  • Background Screening & Drug Testing:Final candidates may be required to successfully complete a background check and/or drug screening, conducted in accordance with applicable laws and regulations.
  • Washington Fair Chance Act Compliance (if applicable):For applicants who reside in or are applying for roles based in Washington State, Recor Medical adheres to the Washington Fair Chance Act. This means we do not inquire about or consider criminal history until after an initial determination has been made that the candidate is otherwise qualified for the role, and we do not automatically exclude individuals based on criminal records.
  • New Hire Training:Allemployees are required to successfully completeRecor training program within their first 90 days of employment as a condition of continued employment.

Radiation Safety Requirement

Certain field-based roles at Recor Medical require work in environments where radiation sources (e.g., x-ray equipment) are in use. Employees in these roles will be issued a personal dosimetry badge to monitor occupational exposure and are required to wear it in accordance with company policy and applicable regulatory standards. This program is designed to ensure compliance with federal and state regulations and to maintain radiation exposure at levels that are As Low As Reasonably Achievable (ALARA). Additional guidance and protective equipment, as necessary, will be provided as part of onboarding and ongoing safety training.


Respecting your privacy is an essential part of the Company's privacy program and we are committed to the proper handling of Personal Information collected or processed in connection with an Applicant's application for employment, a Contract Worker's work, or a Former Employee's employment at Recor. Refer to our Applicant, Contract Worker & Former Employee Privacy Policy for more detail information.