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Real World Evidence Rwe Jobs in Washington (NOW HIRING)

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 ...

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 ...

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 ...

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 ...

This position requires highly motivated problem solvers with a strong track record in real-world evidence generation and scientific publications, advanced methodological and analytical skills, strong ...

Join Our Talent Community

Washington, DC

$22.75 - $30.50/hr

If your expertise lies in market access, reimbursement strategy, policy analysis, data science, real-world evidence or value economics, we want to know you! Join the ADVI Health Talent Community and ...

Join Our Talent Community

Washington, DC · On-site

$22.75 - $30.50/hr

If your expertise lies in market access, reimbursement strategy, policy analysis, data science, real-world evidence or value economics, we want to know you! Join the ADVI Health Talent Community and ...

Apply Early

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Showing results 1-20

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 Washington? The most popular types of Real World Evidence Rwe jobs in Washington are:
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:
Infographic showing various Real World Evidence Rwe job openings in Washington as of July 2026, with employment types broken down into 75% Full Time, and 25% Part Time. Highlights an 75% In-person, and 25% Remote job distribution.
Director, Global Oncology Publications

Director, Global Oncology Publications

AstraZeneca

Gaithersburg, MD • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 28 days ago


AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

16th of 73 rated pharmaceutical


Job description

Location: Boston, Seaport or Gaithersburg, MD
3 days per week in office

Do you have expertise in and passion for Medical Affairs in Oncology? AstraZeneca's vision in Oncology is to help patients by redefining the cancer-treatment paradigm with the bold ambition to eliminate cancer as a cause of death. We are proud to work on groundbreaking science with one of the broadest and deepest Oncology pipelines in the business! Help to advance our pipeline by applying expertise and accelerating our pathway to finding a cure.
What you'll do:
  • Lead the development and execution of the publication strategy and tactical plan for Oncology global clinical studies in humans from Phase Ib-IV, and non-clinical trial sources including health economics and outcomes research, epidemiology, real-world evidence (RWE), payer, and non-interventional studies.

  • Head the development of scientific, clinical and RWE planning data into timely publications for prescribers, payers, and patients through disease state and medicine insights

  • 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 and external alliances

  • Lead external agency partners to ensure the accuracy of publication plan and publication results with respect to time, quality and cost, and ensuring accurate compliance documentation

Required for the role:
  • Relevant university degree (BS/BA) or advanced degree in a scientific or medical field (eg PharmD, PhD, MD)

  • 3+ years publications pharmaceutical experience or 5+ years in medical communications agency

  • Adept at collaborating across multiple functions and hierarchies to develop and execute long-term strategic publication plans on time and on budget

  • Be independent, organized, and able to act as a leader in a fast-paced environment

  • Communicate with collaborators regarding the planning and development of publication deliverables

  • Ensure strict adherence to company policies, industry regulations, and ethical standards in all publications

  • Strong project management skills and ability to collaborate with agency partners

Nice to have:
  • Therapeutic knowledge in oncology

  • Knowledge of publication management systems

  • Certification as a Medical Publication Professional (CMPP) desired

Why AstraZeneca?
At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognizing their potential. Join us on our journey of building a new kind of organization to reset expectations of what a bio-pharmaceutical company can be. This means we're opening new ways to work, pioneering groundbreaking methods, and bringing unexpected teams together. Interested? Come and join our journey.
The annual base pay for this position ranges from $193,000 to $289,900. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
Date Posted
29-Jun-2026
Closing Date
30-Jul-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.

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