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Real World Evidence Intern Jobs (NOW HIRING)

We are seeking a Principal Clinical Scientist / Associate Director of Real-World Evidence & Epidemiology to drive observational evidence strategy for our Early Cancer Detection (ECD) portfolio.

Serve as thought leader and subject matter expert in real-world evidence. Undertake external visibility engagements (conference presentations, webinars, peer reviewed publications and white papers ...

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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 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 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 are the key skills and qualifications needed to thrive as a Real World Evidence Intern, and why are they important?

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.
More about Real World Evidence Intern jobs
What cities are hiring for Real World Evidence Intern jobs? Cities with the most Real World Evidence Intern job openings:
What are the most commonly searched types of Real World Evidence jobs? The most popular types of Real World Evidence jobs are:
What states have the most Real World Evidence Intern jobs? States with the most job openings for Real World Evidence Intern jobs include:
Infographic showing various Real World Evidence Intern job openings in the United States as of June 2026, with employment types broken down into 2% As Needed, 85% Full Time, and 13% Part Time. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution.
Real World Evidence (RWE) Analyst

Real World Evidence (RWE) Analyst

Lancesoft

Santa Monica, CA โ€ข On-site

$70 - $86.33/hr

Full-time

Posted 21 days ago


Job description

Job Description
Job Title: Real World Evidence (RWE) Analyst
Location: 100% Remote
Contract Duration: 06 Months
Pay Range: $70.00 - $86.33 USD hourly on W2

Job Description:
The RWE Analyst will contribute to the Real-World Evidence/Health Economic Outcomes Research (RWE/HEOR) Team as part of an effort to contribute to the strategies of the broader Evidence Generation Team, which will include the conduct of timely, relevant, and rigorous analysis of real-world data (RWD) to address critical research questions and contribute to cross-functional initiatives.
The RWE Analyst will be responsible for developing, reviewing, and providing feedback on study documents, such as protocols and statistical analysis plans, and executing planned data analyses using administrative claims, electronic health record (EHR), and observational registry databases. The RWE Analyst will work closely with project teams to manage timelines and workflows, and to communicate results and updates to internal cross-functional stakeholders, including people from Biometrics, Clinical Operations, and Safety.
The RWE Analyst will have access to real-world databases licensed across Gilead and and act as stewards of Gilead's and best research practices, standards, and methodologies underlying the use of RWE.
Key Responsibilities:
Support development of and provide critical appraisal of study protocols for research projects using RWD (e.G., medical claims, EHR, and observational registry databases)
Lead or support development of statistical analysis plans in collaboration with internal stakeholders (e.G., Biometrics and programming team members)
Conduct data reviews for primary/secondary data collected to ensure quality and reliability
Communicate study results with a broader internal cross-functional audience
Adapt performance metrics and dashboards for RWE projects
Support preparation of reports and/or publication materials (e.G., abstracts, manuscripts)
Support cross-functional initiatives to develop and refine internal procedures, workflows, and best practices
Basic Qualifications
Master s degree in Epidemiology, Biostatistics, Statistics or related discipline from an accredited institution and 4+ years of experience working with a broad range of RWD, in academia, at a contract research organization, or in the biopharmaceutical industry
OR
Bachelor s degree in Epidemiology, Biostatistics, Statistics or related discipline from an accredited institution and 6+ years of experience working with a broad range of RWD, in academia, at a contract research organization, or in the biopharmaceutical industry
Preferred Qualifications:
Master s degree or Doctoral level training in Epidemiology, Biostatistics, Statistics or related discipline from an accredited institution
4+ years of oncology research experience highly preferred
In-depth knowledge of claims-based RWD (e.G., HealthVerity, Optum) and prior experience of using claims-based RWD in oncology research
Experience working with EHRs (e.G., IQVIA, Flatiron) and registry databases
Prior experience of using RWD for RWE in regulatory applications, post-marketing studies, and pharmacovigilance
Experience with external control arm (ECA) methodologies
In-depth understanding of the principles of epidemiologic research methods and statistical concepts in support of the analyses and demonstrated proficiency in statistical analysis programming languages commonly used in life sciences (e.G., SAS, R)
Experience in biopharmaceutical industry
Excellent verbal, written and presentation skills, including the ability to effectively communicate statistical methodology and analysis results
Ability to work independently and collaboratively in a constantly changing, diverse, and matrix environment
Meet Your Recruiter
Medhaj Gajjar

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About LanceSoft

Sourced by ZipRecruiter

Established in 2000, LanceSoft is a Certified MBE and Woman-Owned organization. Lancesoft Inc. is one of the highest rated companies in the industry. We have been recognized as one of the Largest Staffing firms and ranked in the top 50 fastest Growing Healthcare Staffing firms in 2022. Lancesoft offers short- and long-term contracts, permanent placements, and travel opportunities to credentialed and experienced professionals throughout the United States. We pride ourselves on having industry leading benefits. We understand the importance of partnering with an expert who values your needs, which is why we're 100% committed to finding you an assignment that best matches your career and lifestyle goals. Our team of experienced career specialists takes the time to understand your needs and match you with the right job Lancesoft has been chosen by Staffing Industry Analysts as one of the Best Staffing Firms to Work for.LanceSoft specializes in providing Registered Nurses, Nurse Practitioners, LPNs/LVNs, Social Workers, Medical Assistants, and Certified Nursing Assistants to work in Acute Care Centers, Skilled Nursing Facilities, Long-Term Care centers, Rehab Facilities, Behavioral Health Centers, Drug & Alcohol Facilities, Home Health & Community Health, Urgent Care Clinics, and many other provider-based facilities.

Industry

Recruiting and staffing services

Company size

1,001 - 5,000 Employees

Headquarters location

Herndon, VA, US

Year founded

2000

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