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Real World Evidence Rwe Jobs in Washington (NOW HIRING)

Westat

Principal Contracts Manager - Hybrid

Bethesda, MD

$95K - $127K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Experience supporting contracts for clinical research, biomedical research, real-world data (RWD), real-world evidence (RWE), health informatics, and public health programs on behalf of NIH, HHS, CDC ...

ADVI Health LLC

Data Scientist-HEOR

Washington, DC · On-site

$90K - $140K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This position offers the opportunity to apply your analytical expertise to real-world evidence (RWE), health outcomes, and market access challenges while making a measurable impact on how treatments ...

ADVI Health LLC

Data Scientist-HEOR

Washington, DC · On-site +1

$90K - $140K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This position offers the opportunity to apply your analytical expertise to real-world evidence (RWE), health outcomes, and market access challenges while making a measurable impact on how treatments ...

ADVI Health

Data Scientist-HEOR

Washington, DC · On-site

$90K - $140K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This position offers the opportunity to apply your analytical expertise to real-world evidence (RWE), health outcomes, and market access challenges while making a measurable impact on how treatments ...

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All JobsReal World Evidence Rwe JobsReal World Evidence Rwe Jobs in Washington

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 popular job titles related to Real World Evidence Rwe jobs in Washington?

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

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

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

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

Cities in Washington 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 Washington as of August 2026, with employment types broken down into 69% Full Time, 25% Part Time, and 6% Contract. Highlights an 94% In-person, and 6% Remote job distribution.

Epidemiologist

Tunnell Government Services

Bethesda, MD • On-site

Full-time

Posted 7 days ago

Job description

Tunnell Government Services, Inc., is comprised of the industry's leading scientists, medical and technical experts, and human capital and organizational development professionals. We approach all projects as a team and are committed to helping our clients transform and quickly achieve strategic goals. If you are interested in joining an employee-owned company that develops and implements innovative, integrated and differentiated solutions, please click on the links below to find the job that is right for you and contact us.
Epidemiology Subject Matter Expert - Position Description
The mission of the FDA Center for Devices and Radiological Health (CDRH) is to protect and promote the public health. CDRH assures that patients and providers have timely and continued access to safe, effective, and high-quality medical devices and safe radiation-emitting products.
The Office of Clinical Evidence and Analysis within CDRH's Office of Product Evaluation and Quality (OPEQ) provides policy and program support regarding clinical trials, biostatistics, real-world evidence, epidemiological analysis and outreach and collaboration with hospitals and other external stakeholders.
Tunnell Government Services, Inc. is providing professional and scientific services to CDRH with expert consultants with scientific expertise in the regulation and approval and of medical devices. In general, these consultants provide consultation related to supporting medical device reviews (EUA, 510(k), PME and De Novo marketing applications, Pre-submissions); participate in meetings and teleconferences; coordinate meetings with internal and external stakeholders; develop written reviews and correspondence; write detailed documents and reports; and execute other administrative tasks related to CDRH's projects.
Tunnell is seeking a candidate to provide expert consulting services to assist the CDRH with their regulatory responsibilities. This candidate should possess specific expertise and applicable training in epidemiology, as relevant to:
  • Evaluating the safety, effectiveness, and post-market performance of medical devices and radiation-emitting products
  • Analyzing clinical trial data, real-world evidence (RWE), and adverse event reports monitoring the safety and effectiveness of medical devices, under the direction of federal personnel.

Key Duties and Responsibilities
  • Post-Market Surveillance: Monitor medical devices already on the market to detect safety signals, assess risks, and investigate adverse events
  • Clinical Trial & Study Design: Collaborate with biostatisticians and medical officers to review study protocols, clinical evidence, and real-world data (RWD)
  • Regulatory Decision-Making: Use epidemiological methods to guide policy frameworks, ensuring that patients and healthcare providers have timely access to safe and effective devices
  • Risk/Benefit Analysis: Quantify the benefits and risks of innovative medical technologies, including AI and digital health applications

Qualifications
  • The ideal candidate will have a doctorate in an area of study such as Epidemiology, Applied Statistics, or Public Health.
  • Possess several years of experience coordinating, conducting, and/or reviewing epidemiologic studies, surveys, and/or analyses to inform program and policy decisions.
  • Regulatory Knowledge: An understanding of medical device regulations is preferred.
  • The candidate must possess a bachelor's degree (BS) in a relevant field
  • An advanced degree (MD, MS, PhD) in a related/applicable field is strongly preferred.
  • 5-7 years of applicable experience is required, however advanced degrees can substitute for professional work experience
  • Ability to communicate well with others using excellent written and verbal communication skills.
  • Excellent interpersonal skills, with the ability to effectively work both independently and within a team of technical personnel.
  • Proficiency with Microsoft Office Suite (Outlook, Word, Excel, etc.)

Job Type: Full Time
Schedule: Monday through Friday (No Holidays)
Location: This position is 100% telework.
Must be a US Citizen or a Full Green Card holder.
Tunnell strives to hire and retain the most qualified talent. We believe that having employees with different backgrounds and capabilities contributes to the success of our business. To attract qualified applicants, Tunnell posts to a wide variety of job sites. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Please be advised that certain client contracts may outline specific requirements for onsite work. Tunnell employees and/or contractors are expected to comply with all client requirements, including any safety and health protocols.

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