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Real World Evidence Rwe Jobs in North Carolina (NOW HIRING)

COMPASS Pathways

HEOR Science Liaison

Raleigh, NC · On-site +1

The HEOR Science Liaison delivers credible, non-promotional scientific exchange across clinical evidence, real-world evidence (RWE), pharmacoeconomics, and health outcomes to support informed ...

Labcorp

Sr. Business Development Director

Durham, NC · Remote

Bachelor's degree * 5 or more years of experience selling Real World Data (RWD), Real World Evidence (RWE), RWD services, healthcare data solutions, or related offerings directly to pharmaceutical or ...

Labcorp

Sr. Business Development Director

Durham, NC · On-site

Bachelor's degree * 5 or more years of experience selling Real World Data (RWD), Real World Evidence (RWE), RWD services, healthcare data solutions, or related offerings directly to pharmaceutical or ...

Syneos Health Careers

Clinical Value Liaison

Raleigh, NC · On-site

$235K - $246K/yr

... real-world evidence (RWE), health economics and outcomes research (HEOR), and value-based care. The role generates actionable insights that inform Medical Affairs strategy while helping address ...

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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 North Carolina?

The most popular types of Real World Evidence Rwe jobs in North Carolina are:

What are popular job titles related to Real World Evidence Rwe jobs in North Carolina?

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

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

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

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

Cities in North Carolina 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 North Carolina as of August 2026, with employment types broken down into 75% Full Time, and 25% Part Time. Highlights an 75% In-person, and 25% Remote job distribution.

Senior Epidemiological Programmer RWE - Oncology

IQVIA, Inc.

Durham, NC • On-site

$88K - $220K/yr

Full-time

Re-posted 5 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 224 rated it services

Job description

IQVIA is hiring to expand our dedicated Real-World Evidence (RWE) FSP team, working fully within the environment of a prominent pharmaceutical company. This senior data analyst role sits within our Data Science, Analytics, and Technology Solutions (DATS) team and will be responsible for leading the development of datasets and conducting longitudinal analyses for observational studies in the oncology therapeutic area under a single client portfolio.
It is important that this individual has prior experience in observational research utilizing EMR and claims data, particularly in safety analyses, along with a strong statistical programming skillset and experience managing multiple studies and complex analyses. In this role, individuals will have access to real-world databases and will act as stewards of the client's best practices, standards, and methodologies underlying the use of real-world data (RWD).
Essential Functions
  • Lead development of analytic datasets through raw data processing and conduct data checks / cleaning using secondary real world data sources, including claims, EHR, and lab data (must have experience in PharMetrics Plus, Flatiron, or Tempus)
  • Lead the feasibility of real-world data sources to characterize patient population, build patient cohorts, and define and validate key variables specific to study objectives.
  • Conduct and QC analyses, identification of diagnosis and treatment codes and applying statistical methods to handle censor data, confounding, and missing data.
  • Collaborate with epidemiologists to define specifications for descriptive and complex statistics (e.g., longitudinal analysis, survival analysis, regression models) in studies using RWD for oncology research questions, including safety analyses.
  • Develop and QC TFLs for protocols/reports/manuscripts using RWD (e.g. claims and EHR)
  • Support development of other study documents including protocols, statistical analysis plans, and study reports
  • Communicate timelines, progress reports, and results to project team and key stakeholders
  • Provide technical, programming, and statistical expertise and independently bring project solutions to team for complex studies

Qualifications
  • Master's Degree in Biostatistics, Epidemiology, Data Science or related field with 5-8 years relevant experience or PhD with 3 years relevant experience
  • Strong track record of analysis of RWD using claims, EMR, and lab data (Tempus, Flatiron or PharMetrics Plus is preferred)
  • Experience analyzing oncology data and safety outcomes is preferred.
  • Demonstrated proficiency in advanced statistical programming using SAS and/or R, macros, SQL
  • Prior pharmaceutical experience and advanced knowledge of observational research study design and analytic methodologies
  • Excellent analytic and communication skills with attention to detail
  • Ability to effectively manage and prioritize multiple tasks and projects

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $88,300.00 - $220,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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