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Real World Evidence Rwe Jobs in Utah (NOW HIRING)

ICU Medical

Engineer I, Quality

Salt Lake City, UT · On-site

$69K - $90K/yr

Support containment verification, product segregation, evidence collection, DHR/traveler review ... help solve real-world challenges. With the acquisition of Hospira Infusion Systems in 2017 and ...

Bridgerland Technical College

EMS Instructor

Logan, UT · On-site

$23 - $27/hr

This onsite position offers the opportunity to share your real-world experience while teaching ... Model professionalism, ethical decision-making, teamwork, and evidence-based patient care. * Stay ...

Momentous

Product Marketing Manager

Park City, UT · On-site

$161K/yr

... real-world experience to create a portfolio of products designed with one common goal-to help our ... Document and maintain claims, proof points, and supporting scientific evidence used in product ...

Momentous

Product Marketing Manager

Park City, UT

$161K/yr

... real-world experience to create a portfolio of products designed with one common goal-to help our ... Document and maintain claims, proof points, and supporting scientific evidence used in product ...

Leidos

Cybersecurity Analyst

Sunset, UT · On-site

Analyze extensive log files, pivot between diverse datasets, and correlate evidence to support ... real-world scenarios. This includes the ability to communicate technical information clearly and ...

Unavailable

Library Maker Space Assistant

Logan, UT · On-site

... with real-world service and research opportunities. The mission of the Edith Bowen Laboratory ... evidence-based practice; to mentor pre-service teachers through instruction and classroom-based ...

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Real World Evidence Rwe information

What is real world evidence (RWE)?

Real World Evidence (RWE) refers to clinical evidence regarding the usage and potential benefits or risks of a medical product, derived from analysis of real-world data (RWD). This data is collected from sources outside of traditional clinical trials, such as electronic health records, insurance claims, patient registries, and wearable devices. RWE plays a crucial role in understanding how treatments work in routine clinical practice, informing regulatory decisions, and supporting drug development and market access. Organizations use RWE to complement clinical trial data, improving healthcare outcomes and patient care.

How does a real world evidence (RWE) professional collaborate with cross-functional teams?

RWE professionals often work closely with colleagues from epidemiology, health economics, medical affairs, and regulatory affairs to design and execute studies using real-world data. Collaboration is essential, as RWE findings support evidence generation for regulatory submissions, market access, and post-marketing surveillance. Regular meetings, data-sharing sessions, and joint project planning are common, ensuring all stakeholders are aligned on study objectives, methodologies, and data interpretation. This collaborative environment helps translate complex data into actionable insights that support decision-making across the organization.

What are the key skills and qualifications needed to thrive as a real world evidence (RWE) professional?

To thrive as a Real World Evidence (RWE) professional, you need a strong background in epidemiology, biostatistics, and data analysis, often supported by an advanced degree in a relevant scientific field. Familiarity with statistical software (such as SAS, R, or Python), real-world data sources (like EHRs and claims databases), and regulatory guidelines (FDA/EMA) is essential. Strong communication, problem-solving, and cross-functional collaboration skills help convey complex findings to stakeholders and integrate RWE into decision-making. These competencies are crucial for generating credible insights that inform clinical, regulatory, and commercial strategies in the healthcare industry.

What is the difference between Real World Evidence Rwe vs Clinical Data Analyst?

AspectReal World Evidence RweClinical Data Analyst
Required credentialsTypically requires a background in healthcare, epidemiology, or biostatistics, often with a master's or PhDUsually requires a degree in health informatics, biostatistics, or related fields, with similar certifications
Work environmentPrimarily in healthcare, pharmaceutical, or research organizations analyzing real-world dataIn clinical research settings, hospitals, or pharmaceutical companies analyzing clinical trial data
Employer and industry usageUsed by pharma companies, healthcare providers, and research institutions to generate real-world insightsUsed by research organizations, hospitals, and pharma for clinical trial data management and analysis

Real World Evidence Rwe professionals focus on analyzing data from real-world settings like electronic health records and insurance claims, while Clinical Data Analysts primarily work with clinical trial data. Both roles require strong analytical skills and related credentials, but Rwe specialists emphasize real-world data sources to inform healthcare decisions.

What are the most commonly searched types of Real World Evidence Rwe jobs in Utah?

The most popular types of Real World Evidence Rwe jobs in Utah are:

What are popular job titles related to Real World Evidence Rwe jobs in Utah?

For Real World Evidence Rwe jobs in Utah, the most frequently searched job titles are:

What job categories do people searching Real World Evidence Rwe jobs in Utah look for?

The top searched job categories for Real World Evidence Rwe jobs in Utah are:

What cities in Utah are hiring for Real World Evidence Rwe jobs?

Cities in Utah with the most Real World Evidence Rwe job openings:

Real World Evidence Rwe jobs near you
Infographic showing various Real World Evidence Rwe job openings in Utah as of August 2026, with employment types broken down into 58% Full Time, and 42% Part Time. Highlights an 83% In-person, and 17% Remote job distribution.

Engineer I, Quality

ICU Medical

Salt Lake City, UT • On-site

$69K - $90K/yr

Full-time

Posted 5 days ago

ICU Medical rating

7.8

Company rating: 7.8 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

159th of 543 rated manufacturers

Job description


Position Summary:
The Manufacturing Quality Engineer I is an entry/developing role that supports day-to-day manufacturing quality assurance activities in a regulated medical device manufacturing environment. The role assists with NCMR coordination, containment documentation, routine investigation support, CAPA task follow-up, complaint evidence gathering, and continuous improvement actions under the direction of more experienced Quality Engineers.
Essential Duties & Responsibilities:
  • Review new NCMRs for completeness of item, lot/serial, quantity, defect description, source, containment status, attachments, photos, and impacted locations.
  • Support containment verification, product segregation, evidence collection, DHR/traveler review, inspection/test data review, and related NCMR history gathering.
  • Draft routine NCMR investigation summaries, factual complaint support inputs, and recommended next steps for QE II/QE III review.
  • Maintain timely updates in SharePoint, Power Automate, Oracle/ERP, or site trackers and escalate aging records or missing information.
  • Support CAPA administration by collecting objective evidence, updating task status, preparing implementation records, and following up on assigned actions.
  • Recognize and escalate potential CAPA signals, recurrence, complaint severity, field-risk concerns, systemic process-control concerns, or unclear disposition rationale.
  • Provide daily manufacturing-floor support for quality questions, line holds, sort/rework verification, inspection criteria clarification, and procedural adherence as assigned.
  • Participate in defect-reduction, 5S, visual management, Kaizen, PDCA/A3, and quality-health improvement activities.
  • Follow GDP, data integrity, document-control, training, and procedural requirements to maintain audit-ready records.

Knowledge, Skills & Qualifications:
  • Basic understanding of GDP, NCMR workflow, containment, DHR/traveler records, inspection/test data, complaint support, CAPA task support, and regulated manufacturing expectations.
  • Developing skill in 5-Why, fishbone, Pareto, check sheets, basic process mapping, 5S, PDCA/A3, Kaizen participation, and basic risk concepts.
  • Working knowledge of Excel, SharePoint, Oracle/ERP basics, and Power Automate workflow awareness preferred.
  • Ability to communicate clearly, ask for help early, follow through on assignments, and maintain accurate documentation.

Education and Experience:
  • Must be at least 18 years of age.
  • Bachelor's degree from an accredited college or university in Engineering, Science, Quality, Technology, or a related discipline; or equivalent combination of education and relevant manufacturing/quality experience.
  • 0-2 years of quality, manufacturing, engineering, inspection, or regulated-industry experience preferred.
  • Medical device, ISO 13485, FDA QMSR/cGMP, Oracle/ERP, SharePoint, or Power Automate exposure is helpful.
  • Six Sigma and Lean awareness recommended.

Physical Requirements and Work Environment:
  • This role requires both manufacturing and office environment.
  • While working in the manufacturing environment, high-noise areas, radiological hazards, lasers, and/or biological hazards may be encountered.
  • Lift up to 40 lbs unassisted.
  • Typically requires travel less than 5% of the time.

About Us
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

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Benefits

Hours and flexibility

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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

Social media

Twitter

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