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

Senior Statistical Programmer

Irvine, CA ยท On-site

$75 - $98.48/hr

R * Provide hands on statistical programming support for clinical studies, including development and validation of analysis datasets and statistical outputs, in accordance with regulatory and company ...

BCBA Clinical Supervisor

Menifee, CA ยท On-site

$80K - $90K/yr

Conduct developmental skills assessments (e.g., ABLLS-R, AFLS, VB-MAPP) to create and evaluate ... Collaborate with school personnel by observing students, providing written programming and ...

BCBA Clinical Supervisor

Riverside, CA

$77.20K - $94.40K/yr

Conduct developmental assessments (e.g., ABLLS-R, AFLS, VB-MAPP) to create and evaluate ... Collaborate with school staff by observing students, providing programming recommendations, and ...

BCBA Clinical Supervisor

Riverside, CA ยท On-site

$77.20K - $94.40K/yr

Conduct developmental skills assessments, such as ABLLS-R, AFLS, and/or VB-MAPP, to create and ... If applicable, collaborate with school staff by observing students, providing written programming ...

BCBA Clinical Supervisor

San Bernardino, CA ยท On-site

$76.10K - $93K/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 ยท On-site

$77.20K - $94.40K/yr

Conduct developmental skills assessments (e.g., ABLLS-R, AFLS, VB-MAPP) to create and evaluate ... Collaborate with school personnel by observing students, providing written programming and ...

BCBA Clinical Supervisor

Norco, CA ยท On-site

$79.60K - $97.40K/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 ...

BCBA Clinical Supervisor

Riverside, CA ยท On-site

$77.20K - $94.40K/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 ...

BCBA Clinical Supervisor

Rialto, CA ยท On-site

$74.20K - $90.80K/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 ...

BCBA Clinical Supervisor

San Bernardino, CA ยท On-site

$76.10K - $93K/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 ...

BCBA Clinical Supervisor

Anaheim, CA

$77.50K - $94.70K/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 ...

BCBA Clinical Supervisor

San Bernardino, CA ยท On-site

$76.10K - $93K/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 Jun 2, 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:
Senior Statistical Programmer

Senior Statistical Programmer

Lancesoft

Irvine, CA โ€ข On-site

$75 - $98.48/hr

Contractor

Posted 6 days ago


Job description

Job Description
Title: Senior Statistical Programmer
Duration: Jun 8 Dec 31, 2026

Location: Irvine, CA, 92618
Schedule: 1st Shift, 9: 00 AM - 5: 00 PM
TECHNICAL SKILLS
Must Have
  • Base SAS
  • Clinical Data Interchange Standards Consortium (CDISC) Standards
  • Data Manipulation
  • SAS Macros
  • SAS/STAT

Nice To Have
  • Python
  • R

JOB DESCRIPTION
  • Provide hands on statistical programming support for clinical studies, including development and validation of analysis datasets and statistical outputs, in accordance with regulatory and company standards.
  • The Senior Statistical Programmer Contractor is expected to work independently, deliver high quality 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 inspection ready 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 high level objectives and delivering agreed upon 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 within the scope of the contract.

Required Qualifications
Education & Experience
  • Bachelor s degree in Statistics, Mathematics, Computer Science, or a related field with 5+ years of relevant statistical programming experience
    OR
  • Master s degree (or equivalent) in a related field with 3+ years of relevant statistical programming experience
  • Demonstrated experience performing statistical programming in a clinical trials environment (pharmaceutical and/or medical device).

Required Technical Skills
  • Strong hands on 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 inspection ready.
  • Proficiency interfacing SAS outputs with common productivity tools (e.G., Microsoft Excel, Word, PowerPoint).

Required Professional Skills
  • Strong analytical, problem solving, and organizational skills.
  • High attention to detail and commitment to data quality.
  • Clear written and verbal communication skills.
  • Ability to collaborate effectively with cross functional stakeholders, including statisticians and data managers.
  • Ability to manage competing priorities in a fast paced project environment.

Nice to Have Skills
  • Prior participation in regulatory submissions or submission related 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 contract position and does not include formal people management responsibilities.
  • The contractor is expected to adhere to all applicable quality, compliance, and safety requirements relevant to their work.

Meet Your Recruiter
Ippalapalli Ganesh

LanceSoft logo

About LanceSoft

Sourced by ZipRecruiter

Established in 2000, LanceSoft is a Certified MBE and Woman-Owned organization. Lancesoft Inc. is one of the highest rated companies in the industry. We have been recognized as one of the Largest Staffing firms and ranked in the top 50 fastest Growing Healthcare Staffing firms in 2022. Lancesoft offers short- and long-term contracts, permanent placements, and travel opportunities to credentialed and experienced professionals throughout the United States. We pride ourselves on having industry leading benefits. We understand the importance of partnering with an expert who values your needs, which is why we're 100% committed to finding you an assignment that best matches your career and lifestyle goals. Our team of experienced career specialists takes the time to understand your needs and match you with the right job Lancesoft has been chosen by Staffing Industry Analysts as one of the Best Staffing Firms to Work for.LanceSoft specializes in providing Registered Nurses, Nurse Practitioners, LPNs/LVNs, Social Workers, Medical Assistants, and Certified Nursing Assistants to work in Acute Care Centers, Skilled Nursing Facilities, Long-Term Care centers, Rehab Facilities, Behavioral Health Centers, Drug & Alcohol Facilities, Home Health & Community Health, Urgent Care Clinics, and many other provider-based facilities.

Industry

Recruiting and staffing services

Company size

1,001 - 5,000 Employees

Headquarters location

Herndon, VA, US

Year founded

2000

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