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Real World Evidence Rwe Jobs in Colorado (NOW HIRING)

We move quickly, validate assumptions with evidence, and simplify aggressively to deliver systems ... Scientific Rigor and Real-World Impact * Leadership and Growth * Collaborative Culture

Senior Forward Deployed Engineer

Denver, CO · On-site +1

$107K - $147K/yr

Our platform is HIPAA-compliant and designed for the real-world needs of behavioral health teams - from psychologists to ABA therapists. By combining evidence-based care with powerful technology, w ...

Our platform is HIPAA-compliant and designed for the real-world needs of behavioral health teams - from psychologists to ABA therapists. By combining evidence-based care with powerful technology, w ...

Staff Software Engineer

Denver, CO · On-site

$180K - $220K/yr

That evidence might come from: * Designing and shipping production systems * Building products from ... Experience That Is Particularly Relevant, Not Required Exposure to complex or real-world data ...

That evidence might come from: * Designing and shipping production systems * Building products from ... Experience That Is Particularly Relevant, Not Required Exposure to complex or real-world data ...

Apply Early

Engineering Lead - Integrations Platform

Denver, CO · On-site

$105K - $139K/yr

Our platform is HIPAA-compliant and designed for the real-world needs of behavioral health teams - from psychologists to ABA therapists. By combining evidence-based care with powerful technology, w ...

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Real World Evidence Rwe information

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 jobs are there in clinical trials?

Jobs in clinical trials include Clinical Research Coordinators, Clinical Data Managers, Clinical Research Associates, and Study Monitors. These roles involve tasks such as patient recruitment, data collection, monitoring trial progress, and ensuring compliance with regulations, often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications. The work environment is typically in hospitals, research centers, or pharmaceutical companies, with schedules varying from standard to flexible hours.

What is RCT and RWE?

In the context of a Real World Evidence (RWE) role, RCTs (Randomized Controlled Trials) are clinical studies that randomly assign participants to different treatments to assess efficacy, while RWE involves analyzing data from real-world settings like electronic health records and insurance claims to evaluate treatment effectiveness outside controlled trials. Both are important for informing healthcare decisions and regulatory approvals, with RWE complementing RCT data by providing insights from everyday clinical practice.

What is Real World Evidence (RWE) in the healthcare industry?

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.

What are the roles in clinical trials?

In clinical trials, roles include Principal Investigator who oversees the study, Study Coordinators who manage daily operations, Data Managers who handle data collection and analysis, and Regulatory Affairs Specialists who ensure compliance with regulations. These roles require specific skills, certifications, and knowledge of Good Clinical Practice (GCP) guidelines to ensure the trial's integrity and participant safety.

What are the key skills and qualifications needed to thrive as a Real World Evidence (RWE) professional, and why are they important?

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.

How does a Real World Evidence (RWE) professional typically collaborate with cross-functional teams in the pharmaceutical industry?

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 is RWE in clinical research?

Real World Evidence (RWE) in clinical research refers to data collected from real-world settings outside controlled clinical trials, such as electronic health records, insurance claims, and patient registries. RWE helps researchers and healthcare professionals understand how treatments perform in routine practice and supports decision-making for drug development and regulatory approval.
What are the most commonly searched types of Real World Evidence Rwe jobs in Colorado? The most popular types of Real World Evidence Rwe jobs in Colorado are:
What are popular job titles related to Real World Evidence Rwe jobs in Colorado? For Real World Evidence Rwe jobs in Colorado, the most frequently searched job titles are:
What job categories do people searching Real World Evidence Rwe jobs in Colorado look for? The top searched job categories for Real World Evidence Rwe jobs in Colorado are:
What cities in Colorado are hiring for Real World Evidence Rwe jobs? Cities in Colorado with the most Real World Evidence Rwe job openings:
Infographic showing various Real World Evidence Rwe job openings in Colorado as of July 2026, with employment types broken down into 69% Full Time, and 31% Part Time. Highlights an 72% In-person, 14% Hybrid, and 14% Remote job distribution.
Sys VP Clinical and Industry Trials

Sys VP Clinical and Industry Trials

CommonSpirit Health

Englewood, CO • Remote

$140.22 - $252.40/hr

Full-time

Posted 23 days ago


CommonSpirit Health rating

7.1

Company rating: 7.1 out of 10

Based on 512 frontline employees who took The Breakroom Quiz

370th of 877 rated healthcare providers


Job description


Job Summary and Responsibilities

This is a Remote role with travel as needed.

The System Vice President, Clinical and Industry Trials at CommonSpirit Health, will develop a short-term strategy for clinical and industry trials and manage and expand the health system’s clinical trial enterprise, including investigator-initiated research, industry-sponsored trials, and strategic partnerships in alignment with the system-wide research strategy. Under the direction of the Chief Academic and Scientific Officer, the individual in this role will oversee clinical trial operations, including regulatory compliance, budgeting, contracting, and performance functions for clinical and industry trials. As a senior leader within this key area of focus across the research mission, the System Vice President, Clinical and Industry Trials, will further ensure efficient trial activation, patient
recruitment, and data integrity across all sites, and will identify and cultivate strategic relationships with biopharma, medtech, contract research organizations, and academic institutions as applicable.

The System Vice President, Clinical and Industry Trials, will serve as a key liaison with both external entities and CommonSpirit Health research entities and programs, will collaborate closely with key business partners, including compliance, legal, and other relevant functional units within and outside of CommonSpirit, and will serve an integral role in advancing CommonSpirit Health as a leading
learning health system.

Essential Job Responsibilities :


Operational Oversight 

● Develop a short-term strategy for clinical and industry trials in alignment with the long-term research strategy and system research mission.
● Oversee clinical trial operations, including regulatory compliance, budgeting, contracting, and performance metrics.
● Ensure efficient trial activation, patient recruitment, and data integrity across all sites
● Lead efforts to streamline processes and adopt digital tools for trial management
● Apply innovation and change management initiatives to promote efficiency and quality of clinical trials and industry research
● Ensure adherence to federal, state, and institutional regulations and policies in partnership with system and local legal and compliance teams, and with the administration of internal processes for research enterprise risk management
● Collaborate with executive leaders to align operational strategies with the system research mission

Team Leadership

● Manage and lead a team of clinical research coordinators and leaders across the health system
● Drive innovation in trial design, decentralized trials, and real-world evidence generation
● Facilitate access to trials for communities served by the health system
● Monitor emerging trends in clinical research and translate them into actionable strategies
● Promote a culture of accountability, collaboration, and continuous improvement
● Facilitate employee engagement, staff development, and succession planning
● Travel expectations may include site visits, major departmental meetings, periodic system meetings, external conferences/meetings necessary to execute the functions of this position, and as designated by Academic and Scientific Affairs leadership

Stakeholder Engagement
● Collaborate with physician investigators, research coordinators, and administrative leaders to foster a culture of research
● Oversee and deliver education and training to support professional development and research excellence among clinical research coordinators and staff
● Serve as a key liaison with internal/external sponsors, regulatory bodies, and institutional review boards (IRBs)
● Collaborate with key business partners across the health system to enable research continuity, compliance, and effectiveness
● Partner with aligned research entities to facilitate engagement and strategic alignment
● Execute additional duties, special projects, and engagements as assigned by Academic and Scientific Affairs leadership

#LI-CSH

Job Requirements

Minimum Qualifications:

  • M.D. or equivalent medical degree (D.O., MBBS), M.D./Ph.D. or Ph.D. with advanced research certification (e.g., clinical trialist) and/or equivalent work experience as a clinical trialist
  • Minimum of 10 years of progressive senior leadership experience in the academic medical system, health system, or extramural funding agency with a proven track record of success in managing and advancing a large-scale clinical trial program and related research partnerships
  • Deep understanding of FDA regulations, GCP, and clinical trial lifecycle
  • Experience with application of digital health tools, AI in trials, and decentralized trial models
  • Strong familiarity with Epic or other EHR-integrated research platforms

Required Skills, Abilities, and Training

  • Must have direct operational experience in a large, complex academic medical health system and/or extramural funding agency, with proven ability to develop, lead, and implement large-scale research programs for execution in a complex, matrixed healthcare environment
  • Extensive expertise in regulatory and research compliance requirements, frameworks, systems, and processes, including formal advanced certification
  • Demonstrated ability to work with senior executives and leaders to advance strategic goals and priorities across units and to advance organizational mission
  • Exceptional communication, leadership, and strategic planning skills
  • Expert collaborator with the ability to function with diplomacy and excellence in a complex, matrixed health system
  • Ability to lead cross-functional teams and drive change in complex environments
Where You'll Work

Inspired by faith. Driven by innovation. Powered by humankindness. CommonSpirit Health is building a healthier future for all through its integrated health services. As one of the nation's largest nonprofit Catholic healthcare organizations, CommonSpirit Health delivers more than 20 million patient encounters annually through more than 2,300 clinics, care sites, and 137 hospital-based locations, in addition to its home-based services and virtual care offerings. CommonSpirit has more than 157,000 employees, 45,000 nurses, and 25,000 physicians and advanced practice providers across 24 states and contributes more than $4.2 billion annually in charity care, community benefits, and unreimbursed government programs. Together with our patients, physicians, partners, and communities, we are creating a more just, equitable, and innovative healthcare delivery system.


Pay Range
$140.22 - $252.40 /hour

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