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Real World Evidence Intern Jobs in Raleigh, NC (NOW HIRING)

Labcorp

Business Development Director

Durham, NC · Remote

Experience supporting Real World Data (RWD), Real World Evidence (RWE), clinical development ... Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees ...

New

Labcorp

Sr. Business Development Director

Durham, NC · Remote

Experience supporting Real World Data (RWD), Real World Evidence (RWE), clinical development ... Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees ...

IQVIA

RWE Clinical Project Manager (FSP)

Durham, NC · On-site

$93K - $232K/yr

Job Overview IQVIA is hiring a clinical project manager to expand our dedicated Real World Evidence (RWE) FSP team, working fully within the environment of a prominent pharma company. In this role ...

IQVIA

RWE Clinical Project Manager (FSP)

Durham, NC · On-site

$93K - $232K/yr

Job Overview IQVIA is hiring a clinical project manager to expand our dedicated Real World Evidence (RWE) FSP team, working fully within the environment of a prominent pharma company. In this role ...

IQVIA, Inc.

RWE Clinical Project Manager (FSP)

Durham, NC · On-site

$93K - $232K/yr

Job Overview IQVIA is hiring a clinical project manager to expand our dedicated Real World Evidence (RWE) FSP team, working fully within the environment of a prominent pharma company. In this role ...

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 ...

IQVIA

Senior Epidemiological Programmer RWE

Durham, NC · On-site

$88K - $220K/yr

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 ...

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Real World Evidence Intern information

What does a Real World Evidence Intern do?

A Real World Evidence (RWE) Intern supports research teams in collecting, analyzing, and interpreting health data from real-world settings, such as electronic health records, insurance claims, and patient registries. Their work helps organizations understand how medical treatments perform outside of controlled clinical trials. Interns may assist in data management, statistical analysis, literature reviews, and preparing research reports. This role is important for generating insights that inform healthcare decisions, regulatory submissions, and market access strategies.

What are the key skills and qualifications needed to thrive as a Real World Evidence Intern?

To thrive as a Real World Evidence Intern, you generally need a background in life sciences or public health, analytical skills, and coursework in statistics or epidemiology. Familiarity with data analysis tools such as SAS, R, or Python, as well as exposure to healthcare databases, is typically required. Attention to detail, strong communication, and a collaborative mindset are important soft skills for this role. These skills and qualities ensure accurate data interpretation, effective teamwork, and the ability to generate insights that support real-world healthcare decision-making.

What types of projects do Real World Evidence Interns typically work on during their internship?

Real World Evidence Interns often contribute to projects analyzing healthcare data, such as electronic health records and claims data, to generate insights about patient outcomes and treatment patterns. Typical responsibilities may include supporting data cleaning, conducting literature reviews, assisting with statistical analyses, and preparing presentations or reports for cross-functional teams. Interns frequently collaborate with data scientists, epidemiologists, and medical affairs colleagues, gaining exposure to both technical and strategic aspects of real world evidence generation. This hands-on experience helps interns develop analytical skills and a better understanding of how real world data informs healthcare decisions.

What is the difference between Real World Evidence Intern vs Clinical Data Analyst Intern?

AspectReal World Evidence InternClinical Data Analyst Intern
Required CredentialsTypically pursuing or holding a degree in public health, epidemiology, or related fieldsUsually enrolled in or graduated from health informatics, biostatistics, or related programs
Work EnvironmentPharmaceutical companies, healthcare organizations, or research institutions focusing on real-world dataHospitals, clinical research organizations, or pharmaceutical companies analyzing clinical trial data
Employer & Industry UsageUsed in health outcomes research, observational studies, and post-market surveillanceUsed in clinical trial data management, data cleaning, and statistical analysis

The main difference between a Real World Evidence Intern and a Clinical Data Analyst Intern lies in their focus areas. The former concentrates on analyzing real-world data from healthcare settings to inform decision-making, while the latter primarily handles clinical trial data to support research and regulatory submissions. Both roles require strong analytical skills and familiarity with health data, but their specific tasks and data sources differ.

What are the most commonly searched types of Real World Evidence jobs in Raleigh, NC?

The most popular types of Real World Evidence jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Real World Evidence Intern jobs?

Cities near Raleigh, NC with the most Real World Evidence Intern job openings:

Real World Evidence Intern jobs near you
Infographic showing various Real World Evidence Intern job openings in Raleigh, NC as of July 2026, with employment types broken down into 78% Full Time, 16% Part Time, 5% Contract, and 1% Nights. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution.

Senior Epidemiologist, Immunology, RWE (FSP Sponsor Dedicated)

IQVIA

Durham, NC • On-site, Remote

$109K - $273K/yr

Full-time

Re-posted 29 days ago

Key responsibilities

  • Design and conduct observational research studies using real-world data sources.

  • Assess evidence gaps, evaluate safety profiles, and develop evidence strategies to support regulatory and clinical development decisions.

  • Collaborate with cross-functional teams to ensure appropriate epidemiologic approaches are applied to address scientific and business questions.

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 226 rated it services

Job description

Join IQVIA's Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes. In this role, you'll work closely with one sponsor, gaining deep knowledge of their therapies while leveraging IQVIA's global expertise.

Core Function Description:

This role will support the Inflammation, Real World Evidence team, providing scientific and strategic epidemiology support for clinical development and drug safety activities. This role will leverage secondary real-world data (RWD) sources to generate evidence that informs regulatory, safety, and clinical development decisions across the product lifecycle.


Key responsibilities include designing and conducting observational research studies, assessing evidence gaps, evaluating safety profiles, and developing evidence strategies to support regulatory interactions and clinical development programs. The Senior Epidemiologist will collaborate closely with cross-functional teams, including Clinical Development, Safety, Regulatory Affairs, Biostatistics, and Real-World Evidence stakeholders, to ensure appropriate epidemiologic approaches are applied to address critical business and scientific questions.


The ideal candidate will have deep expertise in epidemiologic methods, demonstrated experience working within pharma or biotech, and a thorough understanding of regulatory requirements related to clinical development and safety evidence generation.

This is a fully remote position based in the United States.

Minimum Qualifications

  • Doctoral degree (PhD, ScD, or equivalent) in Epidemiology.

  • 5 to 7 years of epidemiology experience within a pharmaceutical/biotechnology company.

  • Demonstrated experience supporting clinical development and/or drug safety.

  • Strong expertise in observational research methods and the use of commercial healthcare databases such as HealthVerity, Pharmetrics Plus, TriNetX, or similar real-world data assets.

  • Solid understanding of regulatory requirements and evidence needs supporting clinical development, including the generation of evidence to address regulatory questions related to safety profiles and evidence gaps for Phase II and Phase III programs.

  • Proven ability to design, execute, and interpret epidemiologic studies that support regulatory, clinical, or safety objectives.

Preferred Qualifications

  • Experience in Inflammation and Immunology therapeutic areas.

  • Knowledge of disease areas such as Atopic Dermatitis, Asthma, Lupus, Immune Thrombocytopenia (ITP), Autoimmune Hemolytic Anemia, or other immune-mediated diseases.

  • Experience supporting assets within emerging immunology programs.

  • Experience working with primary or hybrid real-world data sources in addition to secondary data sources.

  • Prior experience supporting regulatory submissions or interactions with FDA, EMA, or other global health authorities.

What's in it for you?

  • Be part of a forward-thinking team that helps shape the next generation of evidence-based healthcare.

  • Work hand-in-hand with one leading sponsor, gaining deep expertise in their therapies.

  • Access IQVIA's global network who supports your growth.

This is your chance to make an impact, while building a career that matters.

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 athttps://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 $109,200.00 - $273,000.00. 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.

What IQVIA employees say

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Benefits

Hours and flexibility

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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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