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

Experience with statistical programming such as SAS, R, Python. * Experience with CDISC and CDASH standards. * Strong knowledge and experience in clinical trial design and data analysis, with ability ...

R-112209 Medical Assistant

Lynnwood, WA · On-site

$19.75 - $25.25/hr

The magic we've created lies in Carbon Health's custom EHR and the collaboration among clinical teams, engineers, and designers who work side-by-side to deliver innovation like our hands free AI ...

Analyze hospital inpatient, provider claims, clinical, financial, operational, and population ... Python or R experience * Tableau experience * Experience integrating Power BI with SQL databases ...

Analyze hospital inpatient, provider claims, clinical, financial, operational, and population ... Python or R experience * Tableau experience * Experience integrating Power BI with SQL databases ...

Develop and disseminate a variety of tools designed to access relevant clinical and sample data ... R, Python, Perl, Java, C++) and willingness to learn new programming languages as necessary ...

Showing results 21-40

Clinical R Programmer information

See Seattle, WA salary details

$28

$73

$116

How much do clinical r programmer jobs pay per hour?

As of Aug 6, 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 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 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:
Infographic showing various Clinical R Programmer job openings in Seattle, WA as of August 2026, with employment types broken down into 82% Full Time, and 18% Part Time. Highlights an 88% In-person, 6% Hybrid, and 6% Remote job distribution, with an average salary of $153,327 per year, or $73.7 per hour.

Senior Automation Engineer Aesthetic Medical Device (Bothell, WA)

Bausch Health

Bothell, WA • On-site

$116K - $152K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 26 days ago


Job description

Senior Automation Engineer Aesthetic Medical Device (Bothell, WA)
Job Location: Bothell, Washington, USA
Job Requisition ID: 14957
Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it-where your skills and values drive our collective progress and impact.
The Senior Automation Engineer is responsible for leading the design, development, validation, and implementation of automation systems and equipment to support manufacturing operations. This role ensures product quality, delivery efficiency, and cost optimization while driving continuous improvement in automated processes.
  • Own and execute site-let automation projects end-to-end; serve as Solta technical owner for integrator-led automation projects (URS/specs, design reviews, FAT/SAT, acceptance).
  • Develop and drive best practices around automation equipment design principles and standards.
  • Set Design for Automation (DFA) requirements and work with Product Development to ensure manufacturability of products.
  • Hold design reviews and ensure DFA requirements are met.
  • Collaborate with stakeholders (manufacturing and test engineers, technicians, operators) to develop and execute semi-automation or partial automation projects.
  • Develop and execute process and equipment verification and validation (IQ/OQ/PQ) plans, reports, and associated documentation (requirements, SOPs, training, change control).
  • Develop and implement optical inspections to ensure quality processes.
  • Create and provide requirements to vendors for quoting equipment.
  • Perform Gage R&R analysis on new products and processes.
  • Initiate root-cause analysis and troubleshooting of deployed automation to improve OEE/yield and reduce cost.
  • Consult with leadership on overall automation strategy.
  • Provide technical leadership and mentorship to manufacturing engineers.
  • Act as site automation technical authority.
  • Identify and justify automation projects across labor, quality, risk, and capacity drivers.

Qualifications:
  • BS in Mechanical Engineering or Electrical Engineering, related field, or equivalent experience.
  • Minimum 5 years of experience designing, developing, or implementing automated equipment/systems in a manufacturing or industrial environment.
  • Proven Project Management skills through the delivery of business-critical projects.
  • Proficiency in automation technologies, industrial and collaborative robotics, and vision systems.
  • Demonstrated ability to set up manufacturing lines and processes.
  • Experience assessing process variables utilizing a process failure modes effects analysis (PFMEA).
  • Demonstrated ability to verify and validate production processes and equipment (IQ/OQ/PQ, FAT, SAT).
  • Demonstrated ability to drive production process improvement through equipment, methods, and design.
  • Demonstrated ability to utilize SPC and design of experiments to drive change.
  • Demonstrated ability to drive DFA improvement into product designs during development.
  • Demonstrated ability to utilize and implement lean manufacturing concepts.
  • Experience with Creo or other CAD solid modeling tools.
  • Strong PC skills required - Word, Excel, PowerPoint, etc.

Desired skills:
  • Experience in a capital equipment medical device manufacturing environment.
  • Working knowledge of medical device FDA QSR's and ISO 9001 requirements.
  • Experience with PLC programming
  • Background in RF and laser equipment and/or diagnostic or therapeutic ultrasound.

Language and Verbal Skills
Ability to read, analyze, and interpret engineering specifications, general business periodicals, professional journals, technical procedures, or governmental regulations. Ability to write reports, specifications, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public. Ability to clearly and concisely convey project accomplishments, obstacles, issues, and status to project team members.
Math Skills
Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of plane and solid geometry and trigonometry. Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. Ability to use MS Excel or Minitab to perform calculations and interpret project results/data.
Analytical and Reading Skills
Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. Ability to read regulatory, technical and clinical literature and documents and extract important concepts.
Physical Requirements
While performing the duties of this job, the employee may be required to perform lifting tasks of up to 30 pounds for short durations. Duties of this job may involve standing and/or walking for extended periods of time. Duties also involve daily keyboard data entry. Specific vision abilities required by this job include close vision.
Work Environment
The work environment is office and light manufacturing. The noise level in the work environment is usually moderate. Some light machining and prototyping activities will involve moderate noise levels (i.e. power drill) and moderate dust or debris exposure.
Safety
Solta Medical is committed to the health and safety of our employees. We expect that all employees will perform their responsibilities while maintaining a safe, cooperative, and productive work environment, thus ensuring the health and safety of themselves and others.
The range of starting base pay for this role is $96K-133K. Actual starting pay will be based on a wide range of factors including, but not limited to, relevant skills, experience, qualifications, education and location. In addition to base pay, this position is eligible for participation in either (i) our annual bonus program or (ii) a sales incentive plan.
Benefits package includes a comprehensive Medical (includes Prescription Drug), Dental, Vision, Flexible Spending Accounts, 401(k) with matching company contribution, discretionary time off, paid sick time, stock purchase plan, tuition reimbursement, parental leave, short-term and long-term disability, life insurance, accidental death & dismemberment insurance, paid holidays, employee referral bonuses and employee discounts.
We are an Equal Opportunity Employer. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.

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About Bausch Health

Sourced by ZipRecruiter

Bausch Health Companies Inc. is a global, diversified pharmaceutical company whose mission is to improve people’s lives with our pharmaceutical products. We develop, manufacture and market a range of products primarily in gastroenterology, neurology, dermatology and international pharmaceuticals. With our leading durable brands, we are delivering on our commitments to patients, health care providers, other stakeholders and society as we build an innovative company dedicated to advancing global health.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Laval, QC, CA

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