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Real World Evidence Rwe Jobs in Colorado (NOW HIRING)

Senior Designer

Denver, CO · On-site

$105K - $148K/yr

We're focused on solving complex, real-world challenges where relationships, context, and precision ... You'll also be the primary owner of our design corpus: the structured, evidence-backed ...

Senior Designer

Denver, CO

$105K - $112K/yr

  • Medical

  • Retirement

  • PTO

We're focused on solving complex, real-world challenges where relationships, context, and precision ... You'll also be the primary owner of our design corpus: the structured, evidence-backed ...

Senior Designer

Denver, CO · On-site

$105K - $112K/yr

  • Medical

  • Retirement

  • PTO

We're focused on solving complex, real-world challenges where relationships, context, and precision ... You'll also be the primary owner of our design corpus: the structured, evidence-backed ...

Founding Electrical Engineer

Denver, CO · On-site

  • Medical

  • Life

  • Retirement

  • PTO

We want someone who can take a high level idea and turn it into a certified real world functional ... We will weigh real evidence of ownership above years served. Results speak for themselves. What You ...

Demand Generation Lead

Denver, CO · On-site

$155K - $185K/yr

  • Medical

  • Retirement

  • PTO

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 ...

Senior Network Engineer

Greenwood Village, CO · On-site

$102K - $140K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... the real world-gaining hands-on experience across projects, technologies, and disciplines ... evidence (ServiceNow experience a plus) * 2+ years of Infrastructure-as-Code (IaC) * Extensive ...

Showing results 21-40

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 Colorado?

The most popular types of 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 August 2026, with employment types broken down into 6% Internship, 54% Full Time, 30% Part Time, and 10% Contract. Highlights an 84% In-person, and 16% Remote job distribution.

Medical Science Liaison, Rare Tumors, Great Plains (NV, ID, UT, MT, WY, CO, ND, SD, NE, KS, MN, I...

Alexion Pharmaceuticals

Denver, CO • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 13 days ago


Job description

This is what you will do:

The Medical Science Liaison (MSL) is a field-based scientific expert that strategically supports the medical and scientific objectives of Alexion, AstraZeneca Rare Disease's product/s across the product/s life cycle. The individual is a peer scientific expert who communicates accurate and applicable science to Healthcare Practitioners (HCPs) within a geographic area. The individual manages and maintains collegial and professional relationships with HCPs and Key Opinion Leaders (KOLs) and identifies and facilitates collaboration opportunities with Alexion, AstraZeneca Rare Disease. The MSL combines strong business acumen and clinical expertise and serves as a peer-to-peer liaison internally to Medical Directors, USMA Leadership Team, cross-functional partners and externally (HCPs & KOLs). The MSL should be able to identify problems early on, seek appropriate help and counsel to work past any barriers, and innovate in order to achieve medical goals and objectives.

You will be responsible for:

HCP relationship management

  • Evaluates their territory to profile and identify the HCPs to engage and build relationships with, as well as identify, important centers of excellence
  • Develops clear, succinct, impactful HCP engagement plans, aligned with medical strategic goals and objectives. Evaluates and refines plans as needed per the progress against the quarterly focus priorities
  • Gains HCPs' trust and respect by effectively providing and communicating relevant scientific/medical information on the company's products and disease states
  • Gathers and disseminates HCP insights as appropriate internally to help inform medical strategy
  • Develops strong working relationships in different external business settings

Scientific knowledge and training

  • Keeps current with scientific knowledge within assigned products and therapeutic area
  • Supports scientific exchange of product/disease state with external stakeholders (HCPs) as needed
  • Provides relevant scientific information to other internal teams and functions as appropriate
  • Demonstrates a functional understanding of real-world evidence and HEOR

Research & Development

  • Demonstrates a strong understanding of clinical study design and protocols
  • Ensures HCPs and stakeholders receive focused and balanced clinical and scientific information
  • Develops expertise in applicable research outcomes to credibly conduct effective discussion with HCPs
  • Supports applicable externally sponsored research and clinical trials, as appropriate

US Healthcare system knowledge

  • Acquires knowledge of the current US healthcare system environment and its impact on the rare disease ecosystem
  • Builds a basic understanding of the foundations of managed markets
  • Acquires a basic understanding of the flow of information in managed care and government organizations

You will need to have:

Minimum Education

  • MD, PharmD, or PhD in biological sciences strongly preferred
  • Clinical experience in a relevant therapeutic area OR track record of success as an MSL

Minimum Experience

  • Industry experience is preferred but not mandatory; if no industry experience, therapeutic area experience is preferred

Specific Knowledge, Skills, and Abilities

  • Has excellent communication skills (oral and written)
  • Energetically embraces responsibilities and demonstrates the ability to achieve goals
  • Has a strong personal initiative
  • Functions well as part of a cross-functional team
  • Exhibits excellent time management
  • Able to work independently
  • Demonstrates leadership skills and high-level job competencies

Additional Role Requirements

  • Office is home based. Travel within region 3-4 days per week with 1-2 office days per week
  • Person should be able to travel minimum ~70% time
  • Required travel to medical meetings, team meetings and other group meetings (including possible weekends, as dictated by conference schedule)
  • Candidate is required to live within the territory
  • The duties of this role are generally conducted in a field environment. As is typical of a field-based role, employees must be able, with or without an accommodation, to travel by public transportation, automobile, train, or plane; work comfortably in a clinical setting; use a computer; engage in communications via phone, video, and electronic messaging; problem solve; engage in complex and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours
  • At AstraZeneca, we are taking bold action on climate because we recognize the connection between healthy people and a healthy planet. As part of our flagship Ambition Zero Carbon program, we have committed to a fully electric vehicle (EV) fleet by the end of 2025, which means that all of our drivers will be assigned an EV. Ability to travel within territory on a regular basis which will include frequent overnight and weekend travel. Valid driver's license and clean driving record required).
  • All activities should be conducted per Alexion, AstraZeneca Rare Disease policies.

The annual base pay (or hourly rate of compensation) for this position ranges from $152,454 to $228,680. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.

Date Posted

03-Aug-2026

Closing Date

23-Aug-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.