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Clinical R Programmer Jobs in Riverside, CA (NOW HIRING)

BALT Group

Senior Process Engineer

Irvine, CA · On-site

$111.60K - $144.40K/yr

... clinical affairs, and regulatory compliance, is responsible for supporting and continuously ... R), and the U.S. Food and Drug Administration (FDA) Quality System Regulation (QSR) and Current ...

BALT Group

Senior Process Engineer

Irvine, CA · On-site

$111.60K - $144.40K/yr

... clinical affairs, and regulatory compliance, is responsible for supporting and continuously ... R), and the U.S. Food and Drug Administration (FDA) Quality System Regulation (QSR) and Current ...

Medtronic

EP Mapping Specialist - CAS

Santa Ana, CA · On-site

In this dynamic role,you'llwork alongside a collaborative team of clinicians, engineers, physicians ... F.R. 214.2(h)(4)(iii)(A) is required. Physical Job Requirements The above statements are intended ...

Medtronic

EP Mapping Specialist - CAS

Corona, CA · On-site

In this dynamic role,you'llwork alongside a collaborative team of clinicians, engineers, physicians ... F.R. 214.2(h)(4)(iii)(A) is required. Physical Job Requirements The above statements are intended ...

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Clinical R Programmer information

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$25

$67

$107

How much do clinical r programmer jobs pay per hour?

As of Jun 3, 2026, the average hourly pay for clinical r programmer in Riverside, CA is $67.58, according to ZipRecruiter salary data. Most workers in this role earn between $55.91 and $76.49 per hour, depending on experience, location, and employer.

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

To thrive as a Clinical R Programmer, you need a solid background in statistics, R programming, and clinical trial data analysis, often supported by a degree in statistics, biostatistics, or a related field. Expertise in SAS, CDISC standards (SDTM/ADaM), and familiarity with clinical data management systems are commonly required. Attention to detail, problem-solving skills, and effective communication enable you to interpret data accurately and collaborate with cross-functional teams. These skills are vital for ensuring reliable statistical outputs that support regulatory submissions and data-driven decisions in clinical research.

What are some common challenges faced by Clinical R Programmers when working with clinical trial data?

Clinical R Programmers often encounter challenges such as handling large and complex datasets, ensuring strict compliance with regulatory standards (like CDISC SDTM and ADaM), and maintaining data integrity throughout the analysis process. Collaboration can be demanding, as programmers must frequently coordinate with biostatisticians, data managers, and clinical teams to interpret data requirements and resolve discrepancies. Staying updated with evolving industry guidelines and managing tight project timelines are also common aspects of the role.

What are Clinical R Programmers?

Clinical R Programmers are professionals who use the R programming language to manage, analyze, and visualize clinical trial data in the pharmaceutical, biotech, or healthcare industries. They play a key role in preparing statistical reports, generating tables, listings, and figures (TLFs), and ensuring data integrity for regulatory submissions. Clinical R Programmers collaborate with statisticians, data managers, and clinical teams to ensure the accuracy and compliance of clinical trial results with industry standards and regulatory requirements.

What is the difference between Clinical R Programmer vs Clinical SAS Programmer?

AspectClinical R ProgrammerClinical SAS Programmer
Required CredentialsTypically requires a degree in statistics, biostatistics, or related field; proficiency in R programmingUsually requires a degree in statistics, biostatistics, or related field; proficiency in SAS programming
Work EnvironmentOften works in research-focused settings, academia, or biotech companies using open-source toolsCommonly employed in pharmaceutical companies, CROs, and clinical trial data analysis using SAS
Industry UsageGrowing in popularity for data analysis and visualization in clinical researchStandard in clinical trial data management and regulatory submissions

While both roles involve programming for clinical data analysis, Clinical R Programmers focus on using R for statistical analysis and visualization, whereas Clinical SAS Programmers primarily use SAS for data management and reporting. The choice depends on the company's preferred tools and project requirements.

What are popular job titles related to Clinical R Programmer jobs in Riverside, CA? For Clinical R Programmer jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Clinical R Programmer jobs in Riverside, CA look for? The top searched job categories for Clinical R Programmer jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Clinical R Programmer jobs? Cities near Riverside, CA with the most Clinical R Programmer job openings:
Clinical R Programmer jobs near you
Senior DQA Engineer

Senior DQA Engineer

ZOLL Medical Corporation

Irvine, CA • On-site

Full-time

Posted 22 days ago

Job description

Acute Care TechnologyAt ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions.
The Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally. Products include AEDs, trauma kits, ventilators, temperature management solutions, and more. Our dedicated employees take pride in their commitment to improving patient outcomes while delivering world-class customer service.
At ZOLL, you won't just have a job. You'll have a career-and a purpose.
Join our team. It's a great time to be a part of ZOLL!
Job Summary
This position reports to the Manager, Design Quality Assurance (DQA) and provides validation test development, execution and results tracking for assigned projects in R&D. The Senior DQA Engineer will be a hands-on participant in his/her assigned product development projects and will conduct functional testing on all ZOLL deliverables, from stand-alone code to complete products and systems. As an integral development team member, the Senior DQA Engineer will be an active participant in, and in some cases lead Test Plan reviews with others in R&D. He/she will provide test recommendations to others in DQA and to the development team as needed; especially to junior members of the DQA group. The Senior DQA Engineer will also be an active participant in product and subsystem requirements development ensuring that all product requirements are testable.
Essential Functions
  • Implementing, reviewing and creating validation/verification test cases and test plans, both for DOA and the development teams.
  • Perform all testing as assigned.
  • Identifying, reporting, and following up on test failures and observed defects.
  • Work with the product development teams to isolate failure modes and capture methods to reproduce product problems.
  • Reviewing and creating new/enhanced product requirements to ensure that the products are testable and meet both written and implied requirements.

Required/Preferred Education and Experience
  • BS, Software Engineering, Electrical Engineering, Biomedical Engineering or equivalent, Advanced Degree preferred
  • 5+ years' experience testing in a system product development environment, knowledge and exposure to HW, SW and Mechanical disciplines, at least 2 years testing in the Medical Device industry required

Knowledge, Skills and Abilities
  • Clear understanding of effective software test design especially as it relates to system level testing of embedded systems
  • Working knowledge of Medical Device industry standards
  • Demonstrated accomplishments in the development of software and hardware testing processes and programs
  • Working knowledge of the underlying biomedical principles and understanding of how the products are used under clinical conditions.
  • Proficient with MS/Office, demonstrated ability to learn and use software engineering tools and applications in MS Windows and Linux environments
  • Excellent written, verbal and interpersonal skills

ZOLL is a fast-growing company that operates in more than 140 countries around the world. Our employees are inspired by a commitment to make a difference in patients's lives, and our culture values innovation, self-motivation and an entrepreneurial spirit. Join us in our efforts to improve outcomes for underserved patients suffering from critical cardiopulmonary conditions and help save more lives.
The annual salary for this position is:
$108,100.00 to $133,000.00
This position is eligible for an annual bonus in accordance with the company's bonus plan. Factors which may affect starting salary include geography, skills, education, experience, and other qualifications of the successful candidate. Details of ZOLL's comprehensive benefits plans can be found at www.zollbenefits.com.
Applications will be accepted on an ongoing basis until this position is filled. For fully remote positions, compensation will comply with all applicable federal, state, and local wage laws, including minimum wage requirements, based on the employee's primary work location.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, disability, or status as a protected veteran.
ADA: The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990.

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