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

Manager of Education

Corona, CA · On-site

$56.37 - $84.55/hr

... R e p o r t i n g to Director of Clinical Operations (DCOP), the Manager of Education i s ... Diverse programming to expand your experience. * HealthStream online learning catalogue with plenty ...

BCBA Clinical Supervisor

Menifee, CA · On-site

$80K - $90K/yr

Conduct developmental skills assessments, such as ABLLS-R, AFLS, and/or VB-MAPP, to create and ... programming and behavioral recommendations, implementing training as necessary, and offering ...

BCBA Clinical Supervisor

Riverside, CA · On-site

$77K - $94K/yr

Conduct developmental skills assessments, such as ABLLS-R, AFLS, and/or VB-MAPP, to create and ... programming and behavioral recommendations, implementing training as needed, and offering regular ...

BCBA Clinical Supervisor

Santa Ana, CA · On-site

$77K - $94K/yr

Conduct developmental skills assessments, such as ABLLS-R, AFLS, and/or VB-MAPP, to create and ... programming and behavioral recommendations, implementing necessary training, and offering regular ...

BCBA Clinical Supervisor

Riverside, CA · On-site

$87K - $107K/yr

Conduct developmental skills assessments, such as (not limited to) the ABLLS-R, AFLS, and/or VB ... programming and/or behavioral recommendations, implementing training as necessary, and providing ...

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Clinical R Programmer information

See Riverside, CA salary details

$25

$67

$107

How much do clinical r programmer jobs pay per hour?

As of Aug 6, 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 skills and qualifications are needed to be a Clinical R programmer?

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 is a Clinical R programmer?

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 are 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 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:

Principal Statistical Programmer

Becton, Dickinson and Company

Irvine, CA • On-site, Remote

Full-time

Posted 9 days ago


BD rating

7.3

Company rating: 7.3 out of 10

Based on 140 frontline employees who took The Breakroom Quiz

305th of 487 rated machine equipment manufacturers


Job description

We are the people who give possibilities purpose

BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description

Role Purpose

Provide handson statistical programming support for clinical studies, including development and validation of analysis datasets and statistical outputs, in accordance with regulatory and company standards. The Principal Statistical Programmer is expected to work independently, deliver highquality programming deliverables, and collaborate effectively with Biostatistics and Clinical Data Management.

Key Responsibilities

Primary Responsibilities

  • Develop complex analysis datasets, specifications, and summary outputs (tables, listings, figures, and graphs) for inclusion in clinical study reports, regulatory submissions, and internal presentations.

  • Create, modify, and maintain SAS programs that meet regulatory and company standards to ensure efficient programming, reporting, review, and traceability.

  • Perform independent program review and validation, ensuring complete, accurate, and inspectionready documentation in compliance with applicable regulations and internal procedures.

  • Support ad hoc and planned analyses in collaboration with the designated statistician, including responses to data review questions.

  • Partner with Clinical Data Management and Biostatistics to review CRFs, database specifications, edit checks, and data derivations as needed.

  • Proactively identify programming risks, data issues, or efficiency opportunities and communicate them clearly to study team members.

Scope & Level of Independence

  • Works independently with minimal supervision, receiving highlevel objectives and delivering agreedupon outputs.

  • Evaluates alternative programming approaches and applies sound judgment in accordance with regulatory and quality standards.

  • May provide technical guidance or support to other programmers, as appropriate.

  • Responsible for managing assigned programming tasks and timelines.

Required Skills/Experience:

  • Bachelor's degree in Statistics, Mathematics, Computer Science, or a related field or other STEM Field with 5+ years of relevant statistical programming experience
    OR

  • Master's degree (or equivalent) in a related STEM field with 3+ years of relevant statistical programming experience

  • Demonstrated experience performing statistical programming in a clinical trials environment (pharmaceutical and/or medical device).

  • Strong handson experience with SAS programming for clinical trial data including SAS Base, SAS/STAT, and SAS Macros.

  • Proven experience developing and validating:

    • Analysis datasets

    • Tables, listings, and figures

  • Solid understanding of regulatory requirements and guidelines applicable to clinical research (e.g., GCP, ICH, FDA, ISO).

  • Experience with CDISC standards (e.g., SDTM, ADaM).

  • Experience supporting programming deliverables that are inspectionready.

  • Proficiency interfacing SAS outputs with common productivity tools (e.g., Microsoft Excel, Word, PowerPoint).

  • Strong analytical, problemsolving, and organizational skills.

  • High attention to detail and commitment to data quality.

  • Clear written and verbal communication skills.

  • Ability to collaborate effectively with crossfunctional stakeholders, including statisticians and data managers.

  • Ability to manage competing priorities in a fastpaced project environment.

Preferred Skills/Experience

  • Prior participation in regulatory submissions or submissionsrelated deliverables.

  • Experience reviewing or validating programming deliverables from CROs or vendors.

  • Development of SAS macros or tools that improve programming efficiency.

  • Ability to program in other statistical languages such as R or Python.

Additional Information

  • This role is an individual contributor position and does not include formal peoplemanagement responsibilities.

  • The programmer is expected to adhere to all applicable quality, compliance, and safety requirements relevant to their work.

At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.

For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.

Why Join Us?

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you'll discover a culture in which you can learn, grow and thrive.

We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.

To learn more about BD visit https://bd.com/careers.

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.

Required Skills

Optional Skills

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Primary Work LocationUSA CA - Irvine Laguna CanyonAdditional LocationsWork ShiftNA (United States of America)

At BD, we reward, support and develop our associates through our comprehensive Total Rewards program. We are committed to attracting and retaining high quality talent by providing reward and recognition opportunities that promote a performance-based culture, as well as a competitive package of compensation and benefits programs. You can learn more on our career site under "Our Commitment to You."

Our salary or hourly rate ranges reward associates fairly and competitively. We regularly review these ranges and factors, such as location, contribute to the range displayed.

Our pay is based on the role and the necessary skills and education to perform it successfully. The salary or hourly rate offered is determined by the role's specific requirements, including any applicable step rate pay system at the work location. Salary or hourly pay ranges are influenced by labor laws and Collective Bargaining Agreement (CBA) requirements applicable to the work location which may also affect the workplace arrangement of the role.

Salary Range Information

$129,600.00 - $207,400.00 USD Annual

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About BD

Sourced by ZipRecruiter

BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues.

Industry

Medical equipment and supplies manufacturing and manufacturing

Company size

10,000+ Employees

Headquarters location

Franklin Lakes, NJ, US

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