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Real World Evidence Rwe Jobs in Washington, DC (NOW HIRING)

Westat

Principal Contracts Manager - Hybrid

Bethesda, MD · On-site

$95K - $127K/yr

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

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

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

$140K/yr

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

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, DC

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, DC?

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

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

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

Real World Evidence Rwe jobs near you
Infographic showing various Real World Evidence Rwe job openings in Washington, DC as of August 2026, with employment types broken down into 6% Internship, 6% As Needed, 63% Full Time, 19% Part Time, and 6% Contract. Highlights an 81% In-person, 13% Hybrid, and 6% Remote job distribution.

Global Publications Leader, Oncology

Fladger Associates

Gaithersburg, MD • On-site

Contractor

Re-posted 7 days ago

Job description

Gaithersburg, MD
Contract Duration: 12-36 months
Rate: Negotiable

Responsibilities:

  • Excellent employment opportunity for a Global Publications Leader, Oncology in the Gaithersburg, MD area.
  • Position can be remote, but candidates must be able to travel as needed. This would be for onsite meetings as required and also to medical conferences as they are likely to produce presentations and a presence might be needed
  • The Global Publications Leader (GPL), Oncology delivers the strategic publications plan for the oncology franchise and leads a cross-matrix team of Company
  • Due to the importance of this portfolio, you must be an experienced publication professional, ready for new challenges with creative and collaborative problem-solving skills
  • The prominence of this role will provide you with opportunities for significant interactions with senior and global stakeholder in the organization as well as key external stakeholders
  • Leading the development and execution of the publication strategy and tactical plan for global clinical studies in humans from Phase I-IV, and non-clinical trial sources including health economics and outcomes research, epidemiology, real-world evidence (RWE), payer, and non-interventional studies, aligned with a specific medical strategies and objectives
  • Heading the development of scientific, clinical and RWE planning data into timely publications for prescribers, payers, and patients through disease state and medicine insights and leading effective collaboration with cross-functional teams and external alliances
  • Tracking existing publication plans to ensure alignment with evidence plans
  • The day-to-day management of assigned publication plans, delivery of outputs, financial tracking and meeting activities, working closely with all members of the delivery team
  • Developing a thorough understanding of internal and external stakeholders to further the leverage of clinical and RWE studies
  • Manage external agency partners to ensure accuracy of publication plan and publication deliverables with respect to time, quality and cost, and ensuring correct compliance documentation is in place including budgetary responsibilities

Experience

  • Relevant University Degree (BS/BA) OR Advanced Degree in a Scientific or Medical discipline (e.g., PharmD, PhD, MD)
  • Strong Medical Affairs experience is required, preferably Publication experience as well
  • Oncology experience is highly desired
  • 5-10 years of experience
  • Poise in Senior Leader engagement
  • The ability to appreciate and work within a large strategic framework, while maintaining strong attention to detail and compliance to global publications ethical standards and company publications policy and SOPs
  • Demonstrated performance, budget, and resource management skills in a global organization
  • Ability to understand and adhere to good publication practices and relevant guidelines on and scientific data communication, such as ICMJE, GPP3, company policy and SOPs
  • Strong therapeutic knowledge in oncology
  • Experience in collaboration within a Medical Affairs organization
  • Broad understanding of drug development process
  • Experience in medical communications gained through working in the pharmaceutical industry or a medical communications agency
  • Demonstrated ability to establish and maintain professional relationships with external experts, investigators, journal editors and publishers and professional bodies
  • Flexibility and adaptability to manage long-term activities in a constantly changing internal and external environment
  • Working knowledge of Datavision publication management systems
  • Medical Writers are not good fits for this position and will not be considered