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Clinical Programmer Jobs (NOW HIRING)

Position Summary The Clinical Programmer II at Recor Medical develops and maintains advanced programming solutions for clinical trial data management, analysis, and reporting. This role requires ...

Position Summary The Clinical Programmer II at Recor Medical develops and maintains advanced programming solutions for clinical trial data management, analysis, and reporting. This role requires ...

Clinical Applications Programmer II Salary Range : $60,000-70,000 Location : Baltimore, MD About Pharmaron Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping ...

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

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

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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$102

How much do clinical programmer jobs pay per hour?

As of Aug 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 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 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.

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.

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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?

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Infographic showing various Clinical Programmer job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.

Clinical Programmer II

Palo Alto, CA โ€ข On-site

Recor Medical
Medical Equipment and Supplies Manufacturingย โ€ขย 11 - 50 employees

Full-time

Posted 15 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 Clinical Programmer II at Recor Medical develops and maintains advanced programming solutions for clinical trial data management, analysis, and reporting. This role requires strong proficiency in R and/or SAS and understanding of clinical trial processes and operational metrics. Key responsibilities include performing complex data analysis, generating reports, and creating tools to support both clinical research and operational decision-making. The ideal candidate will collaborate with cross-functional teams, mentor junior programmers, and contribute to process improvements. They will demonstrate technical expertise, problem-solving skills, and the ability to work independently and collaboratively, while staying current with industry trends and maintaining high standards of quality and compliance.

Responsibilities and Duties

  • Design, develop, validate, and maintain complex programs to support clinical trial data management processes, including data integration, transformation, and analysis using R, SAS, or other relevant programming languages.

  • Perform advanced data analysis and generate complex reports, tables, listings, and figures to support clinical trial data review, statistical analysis, regulatory submissions, and operational decision-making.

  • Support clinical operational activities by developing and maintaining tools for tracking study progress, site performance, and other key operational metrics, including generating regular reports and dashboards to provide insights into clinical trial operations.

  • Collaborate with cross-functional teams to implement statistical analysis plans and design programming solutions that address specific project requirements.

  • Troubleshoot complex data issues and propose solutions to ensure data integrity and quality throughout the clinical development process.

  • Conduct programming peer reviews, provide technical guidance, and mentor junior programmers to ensure code quality and adherence to standards.

  • Participate in version control using Git and maintain comprehensive documentation for scripts, packages, and applications.

  • Contribute to the development of study documentation, including programming specifications and data management plans.

  • Lead process improvement initiatives to enhance efficiency and quality in clinical programming activities.

  • Stay abreast of emerging trends, technologies, and industry standards (e.g., CDISC) in clinical programming and data management, implementing improvements as appropriate and assisting in preparing for regulatory audits and inspections.

  • Other duties as assigned

Requirements

  • Master's degree in computer science, data science, statistics, life sciences, or related field with 1+ years of experience; or a Bachelor's degree in these fields with 2+ years of professional experience in Clinical Programming, data visualization, business intelligence, or analytics roles.

  • Strong proficiency in R and/or SAS, with experience in other relevant programming languages and tools (e.g., Python, SQL).

  • Demonstrated ability to identify and resolve performance bottlenecks and optimize code for efficiency and scalability.

  • Experience in extracting, cleaning, transforming, and loading data from diverse sources, managing datasets, and ensuring data quality and integrity.

  • Understanding of clinical trial processes and data flow from study setup to database lock.

  • Working knowledge of clinical trial data standards (e.g., CDISC SDTM, ADaM) is strongly preferred.

  • Experience with or understanding of clinical trial operations and associated metrics is highly desirable.

  • Excellent problem-solving and analytical skills, with the ability to translate complex requirements into efficient programming solutions.

  • Experience with version control systems (e.g., Git) and collaborative development practices.

  • Familiarity with tools and techniques for visualizing operational data and creating interactive dashboards (e.g., Tableau, Power BI) is a plus.

  • Ability to mentor junior team members, including conducting code reviews and providing technical guidance.

  • Strong written and verbal communication skills, with the ability to explain technical concepts to non-technical stakeholders.

  • Demonstrated ability to work independently and collaboratively in a fast-paced environment.

  • Commitment to continuous learning and staying updated with emerging trends in clinical programming and data analysis.

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: $122,857 - $132,796 (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.