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Clinical R Programmer Jobs in Tooele, UT (NOW HIRING)

Senior Engineer, Manufacturing

Salt Lake City, UT · On-site

$88.10K - $120.50K/yr

Six-Sigma Methodology (DOE, Process Capability, Gage R&R, etc.) * Knowledge of the Medical Device ... Dedicated and non-dedicated IV sets and needlefree connectors clinically proven to provide an ...

R-1948 Description About Norstella: Norstella is a premier and critical global life sciences data ... Match and recruit patients for clinical trials * Identify and address barriers to therapies ...

R-1950 Description About Norstella: Norstella is a premier and critical global life sciences data ... Match and recruit patients for clinical trials * Identify and address barriers to therapies ...

Biostatisticians

Salt Lake City, UT · On-site

$19.70 - $22/hr

... clinical research data. Perform statistical design, modeling, and analysis. Provide statistical ... Consult with scientists and engineers to ensure proper use of statistical methodology and ...

Clinical R Programmer information

See Tooele, UT salary details

$23

$60

$96

How much do clinical r programmer jobs pay per hour?

As of Jun 4, 2026, the average hourly pay for clinical r programmer in Tooele, UT is $60.81, according to ZipRecruiter salary data. Most workers in this role earn between $50.34 and $68.85 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 cities near Tooele, UT are hiring for Clinical R Programmer jobs? Cities near Tooele, UT with the most Clinical R Programmer job openings:
Senior Engineer, Manufacturing

Senior Engineer, Manufacturing

ICU Medical

Salt Lake City, UT

$88.10K - $120.50K/yr

Full-time

Posted 12 days ago


ICU Medical rating

7.8

Company rating: 7.8 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

163rd of 515 rated manufacturers


Job description

Position Summary 

The Senior Manufacturing Engineer will support the ICU Manufacturing Engineering Department and report to the Manufacturing or Product Engineering Manager. The Senior Manufacturing Engineer is responsible for owning and driving process improvements through adherence to established design control processes, good engineering and documentation practices. The key responsibility of this position is to exercise judgement and take action while adhering to defined procedures during project support & improvements.

Essential Duties & Responsibilities

  • Functional area tasks and responsibilities
    • Day to day
      • Initiate and manage projects with adherence to program-management guidelines
      • Own and manage CAPA tasks and deliverables (Corrective and Preventive)
      • Lead vendor assessment and review of materials/machine technical information
      • Identify and implement process and product modifications to improve manufacturability and impact on automation equipment
      • Consult with Product and Molding Engineers on in-process non-conformances
      • Process technical expert for multiple manufacturing production lines
      • Create and edit documents to support Production
      • Work with Quality Engineers on qualification activities for new or modified processes and equipment
    • Long term expectations
      • Spearhead initiatives for continuous process improvements
      • Develop a broad understanding from start to end of the product manufacturing process in the company
      • Perform design assessments, active participation in design reviews and risk management processes
      • Network with senior internal and external personnel

Knowledge, Skills & Qualifications

  • Substantial knowledge in one or more key process areas: automation, medical-device assembly, controls, etc
  • Understanding of strength of materials, plastic injection molding, fixturing, testing, and process control techniques
  • Six-Sigma Methodology (DOE, Process Capability, Gage R&R, etc.)
  • Knowledge of the Medical Device Industry and familiarity with FDA QSR regulations
  • Solid works knowledge to interpret part dimensions, sectional views, conduct mates and build assemblies
  • Technical writing competency.

Education and Experience 

  • Must be 18 years of age
  • Bachelor's degree from an accredited college or university (Engineering, Technology, or STEM)
  • Medical Device Experience is a must
  • 8 years combined experience in the Medical Device or Engineering Industry
  • Advanced Degree may substitute for experience

Physical Requirements and Work Environment 

  • While performing the duties of this job, the employee is regularly required to talk or hear
  • This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines
  • Work is performed in a clean room environment
  • While performing the duties of this job, the employee may be required to sit or stand for long periods of time
  • Must be able to occasionally move and lift objects of up to 25 lbs

ICU Medical has consistently provided you with clinical innovations that help solve real-world challenges.

With the acquisition of Hospira Infusion Systems in 2017 and Smiths Medical in 2022, we are now a global market leader with a complete line of clinically-essential IV therapy and high-value critical care products for hospital, alternate site, and home care settings.

We're ready to bring you consistent quality, innovation, and value in more areas than ever. Our focus allows us to bring you:

  • Dedicated and non-dedicated IV sets and needlefree connectors clinically proven to provide an effective barrier against bacterial transfer and colonization.
  • The industry's broadest IV smart pump offering covering large volume, pain management, and ambulatory needs.
  • IV medication safety software providing full IV-EHR interoperability with the highest customer satisfaction and compatibility with more EHR systems than any other company.
  • Significant US IV solutions manufacturing and supply capabilities.

ICU Medical EEO Statement:

ICU Medical is committed to being an Equal Opportunity Employer. We ensure that all qualified applicants receive fair consideration for employment regardless of race, color, nationality or national origin, ethnicity, sex, gender, religion or belief, marital or civil partnership status, sexual orientation, pregnancy or maternity, age, disability, or protected veteran status. 

If you are an individual with a disability and need reasonable accommodation to participate in the employment selection process, please contact us at humanresources@icumed.com. We are committed to providing equal access and opportunities for all candidates.

ICU Medical EEO Policy Statement

Know Your Rights: Workplace Discrimination is Illegal Poster

ICU Medical CCPA Notice to Job Applicants


What ICU Medical employees say

Pay

Benefits

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About ICU Medical

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

San Clemente, CA, US

Year founded

1984

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