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Clinical R Programmer Jobs in Seattle, WA (NOW HIRING)

SystImmune, Inc

Clinical Data Associate

Redmond, WA · On-site

$75K - $95K/yr

SAS, Python, and R programming knowledge is a plus. * Familiarity with CDISC standards (CDASH, SDTM ... Eagerness to learn in a fast-paced, clinical-stage biopharmaceutical environment. * Oncology ...

Systimmune

Clinical Data Associate

Redmond, WA · On-site

$75K - $95K/yr

SAS, Python, and R programming knowledge is a plus. * Familiarity with CDISC standards (CDASH, SDTM ... Eagerness to learn in a fast-paced, clinical-stage biopharmaceutical environment. * Oncology ...

Amgen

Biostatistical Prograrmming Manager

Seattle, WA · On-site

... R programming for clinical trial analyses, data manipulation, reporting and visualization preferred Familiarity with additional programming languages and tools such as Python preferred Hands-on ...

SystImmune, Inc

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

Biostatisticians, Statistical Programmers, Medical Monitors, Clinical Scientists, Clinical Project ... Run SAS and/or R programs, review SAS and/or R logs, troubleshoot errors, and generate output.

Systimmune

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

Biostatisticians, Statistical Programmers, Medical Monitors, Clinical Scientists, Clinical Project ... Run SAS and/or R programs, review SAS and/or R logs, troubleshoot errors, and generate output.

Fred Hutch

Clinical Research Coordinator II

Seattle, WA · On-site

$27.50 - $36.75/hr

... outreach, programming, and research. The Research Coordinator will coordinate research and ... The R&RSR is a developing shared resource available to all Consortium research teams to request ...

Pfizer

Manager, Clinical Pharmacology

Bothell, WA · On-site

$106K - $176K/yr

PhD in Pharmacokinetics, Clinical Pharmacology, Pharmacometrics, Engineering or PharmD * Strong ... Hands-on experience with common software tools for PK and PK/PD analyses (e.g., R, NONMEM, Monolix ...

SystImmune, Inc

Clinical Data Analyst, Spotfire

Redmond, WA · On-site

$90K - $130K/yr

Experience with SAS/R, SQL programming, and data manipulation. * Familiarity with clinical trial data standards (CDISC SDTM, ADaM), experience with TLF generation preferred. * Experience integrating ...

Systimmune

Clinical Data Analyst, Spotfire

Redmond, WA · On-site

$90K - $130K/yr

Experience with SAS/R, SQL programming, and data manipulation. * Familiarity with clinical trial data standards (CDISC SDTM, ADaM), experience with TLF generation preferred. * Experience integrating ...

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All JobsClinical R Programmer JobsClinical R Programmer Jobs in Seattle, WA

Clinical R Programmer information

See Seattle, WA salary details

$28

$73

$116

How much do clinical r programmer jobs pay per hour?

As of Jun 25, 2026, the average hourly pay for clinical r programmer in Seattle, WA is $73.71, according to ZipRecruiter salary data. Most workers in this role earn between $61.01 and $83.41 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 does a clinical programmer do?

A clinical programmer develops and maintains software for clinical trials, including programming data collection, validation, and analysis tools. They work with statistical teams to generate reports and ensure data accuracy, often using programming languages like SAS or R in a regulated environment.

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 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.

Is clinical SAS programmer a good career?

A clinical SAS programmer is a specialized role in the healthcare and pharmaceutical industries, focusing on data analysis and reporting using SAS software. It offers stable employment, competitive salaries, and opportunities for advancement, especially with certifications and experience. The role typically requires strong analytical skills and knowledge of clinical trial processes.

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 is the salary of a clinical data programmer?

The salary of a clinical data programmer typically ranges from $70,000 to $100,000 annually, depending on experience, location, and certifications. Entry-level positions may start lower, while experienced professionals with advanced skills in SAS, R, or SQL can earn higher salaries. Many roles also offer benefits such as health insurance and flexible schedules.

Which is better, CDM or SAS?

For a Clinical R Programmer, SAS is a widely used statistical software in clinical trials and regulatory submissions, offering robust data management and analysis capabilities. CDM (Clinical Data Management) refers to the process of handling clinical data, often using tools like SAS or dedicated CDM systems; the choice depends on project needs, but SAS proficiency is highly valued in the field.
What are popular job titles related to Clinical R Programmer jobs in Seattle, WA? For Clinical R Programmer jobs in Seattle, WA, the most frequently searched job titles are:
What job categories do people searching Clinical R Programmer jobs in Seattle, WA look for? The top searched job categories for Clinical R Programmer jobs in Seattle, WA are:
Clinical R Programmer jobs near you
Infographic showing various Clinical R Programmer job openings in Seattle, WA as of June 2026, with employment types broken down into 11% As Needed, 2% Full Time, 84% Part Time, 1% Temporary, and 2% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $153,327 per year, or $73.7 per hour.
Clinical Data Associate

Clinical Data Associate

SystImmune, Inc

Redmond, WA • On-site

$75K - $95K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 20 days ago

Job description

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
The Clinical Data Associate (CDA) supports the Clinical Data Manager in executing data management activities across clinical trials, with a primary focus on Phase 3 and other large-scale studies. The CDA will gain hands-on experience across the full DM lifecycle while working under the guidance of senior data management staff.
This role is full-time onsite in Redmond, WA. Please note that SystImmune plans to relocate to a new facility in Bothell, WA in the fall.
Responsibilities:
  • Support the CDM in day-to-day data management activities across study start-up, maintenance, and close-out, including tracking open queries and data cleaning timelines.
  • Assist in the development and review of DM documents such as Data Management Plans, CRF Completion Guidelines, and data review plans using established templates and standards.
  • Perform data review activities including query generation, query resolution follow-up, and non-system edit check output review under CDM oversight.
  • Assist with SAE reconciliation and non-CRF data reconciliation activities, escalating issues to the CDM as appropriate.
  • Support medical coding activities using MedDRA and WHO Drug dictionaries, coordinating with the CDM and CRO for medical review.
  • Run and review SAS and/or R programs and data listings as directed; assist in troubleshooting basic programming errors under CDM guidance.
  • Perform UAT (User Acceptance Testing) of EDC systems and edit checks per provided specifications and test scripts.
  • Assist in tracking and coordinating CRO/vendor deliverables, flagging risks or delays to the CDM.
  • Contribute to data quality monitoring by reviewing metrics reports and flagging trends or anomalies to the CDM.
  • Support database lock activities by assisting with lock checklists, outstanding query resolution, and coordination tasks.
  • Participate in the development and review of DM SOPs and process improvement initiatives.
  • All other duties as assigned.

Qualifications:
  • BA or BS in life sciences, health informatics, or a related field.
  • 1-3 years of relevant clinical data management or clinical research experience; equivalent internship or co-op experience in a clinical or pharma setting will be considered.
  • Exposure to a Clinical EDC system (e.g., Medidata Rave, Veeva EDC) preferred.
  • SAS, Python, and R programming knowledge is a plus.
  • Familiarity with CDISC standards (CDASH, SDTM) and GCP guidelines preferred; willingness to develop deep knowledge required.
  • Detail-oriented with strong organizational and time management skills.
  • Effective written and verbal communication skills; ability to work cross-functionally.
  • Eagerness to learn in a fast-paced, clinical-stage biopharmaceutical environment.
  • Oncology experience or interest a plus.

Compensation and Benefits:
The expected base salary range for this position is $75,000 - $95,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate's level qualifications, experience, and skills.
While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

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