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Clinical R Programmer Jobs in Santa Ana, CA (NOW HIRING)

Jj

Associate Director of Stats Programming

Irvine, CA · On-site

... and R programmers in the Medical Devices Sector. This individual will be accountable for the programming of statisticaldeliverables for pre- and post-market global clinical trials across all ...

Lancesoft

Senior Statistical Programmer

Irvine, CA · 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 ...

Intercare Therapy

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 ...

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Clinical R Programmer information

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How much do clinical r programmer jobs pay per hour?

As of Jun 1, 2026, the average hourly pay for clinical r programmer in Santa Ana, CA is $67.40, according to ZipRecruiter salary data. Most workers in this role earn between $55.77 and $76.30 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 Santa Ana, CA? For Clinical R Programmer jobs in Santa Ana, CA, the most frequently searched job titles are:
What job categories do people searching Clinical R Programmer jobs in Santa Ana, CA look for? The top searched job categories for Clinical R Programmer jobs in Santa Ana, CA are:
What cities near Santa Ana, CA are hiring for Clinical R Programmer jobs? Cities near Santa Ana, CA with the most Clinical R Programmer job openings:
Clinical R Programmer jobs near you
Infographic showing various Clinical R Programmer job openings in Santa Ana, CA as of May 2026, with employment types broken down into 82% Full Time, 12% Part Time, and 6% Contract. Highlights an 76% In-person, and 24% Remote job distribution, with an average salary of $140,198 per year, or $67.4 per hour.
Manager, Clinical Programming

Manager, Clinical Programming

Arrowhead Pharmaceuticals

Los Angeles, CA

$120K - $140K/yr

Full-time

Posted 16 days ago

Job description

Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.

Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.

Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.

The Position

We are seeking a manager for clinical programming to join our growing biometrics team to support clinical studies across Arrowhead's expanding portfolio. This is an exciting opportunity for a candidate trained in SAS programming and data analysis is who has some prior experience working as a clinical or statistical programmer, preferably within a CRO or a similar group. Prior management experience is not needed. They will initially contribute their expertise in the area of data management/clinical or statistical programming, with a goal to develop as a lead within clinical programming.

Responsibilities

  • Develop, and execute edit checks and patient profile software or programs for clinical trials;
  • Develop and execute data listing programs used by data managers, safety surveillance, medical or clinical operations personnel;
  • Collaborate with data management to ensure appropriate data collection and reporting. Participate in study team meeting and support data management activities;
  • Program and deliver results on time for ad-hoc data programming requests;
  • Define and help implement statistical computing environment, specifically SAS server setup and work practices;
  • Support statistical programming, from raw data to ADaM, of efficacy and safety evaluation;
  • Interface with CRO and perform quality audits on CRO outputs. Review outputs provided by CROs for accuracy and consistency with the programming specs
  • Assist in efforts to identify, develop, and implement departmental standards, applications, processes and training; and
  • Develop or support standard operation procedure preparation.

Requirements

  • Bachelor's degree in life sciences or technical field;
  • At least 5 years' experience of SAS programming for clinical trials;
  • Working knowledge of SAS, including complex data manipulation, data presentation and output deliver systems;
  • Prior experience implementing edit checks and patient profiles on active clinical trials; and
  • Excellent verbal and written communication skills.

Preferred

  • Familiarity with CDISC standards, derivation of SDTM and ADaM specifications;
  • Data management experience;
  • Proficiency in R; and
  • CRO experience.
California pay range
$120,000—$140,000 USD

Arrowhead provides competitive salaries and an excellent benefit package.

Candidates must have current, valid authorization to work in the country where this role is located.

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