ZipRecruiter

Log In

1

Internship Real World Evidence Rwe Jobs (NOW HIRING)

Datavant

Client Partner, Real-World Evidence

You will serve as a trusted advisor on the use of real-world data (RWD) and RWE to support ... evidence generation requirements. The ideal candidate is comfortable leading complex, multi ...

next page

Showing results 1-20

All Jobsinternship JobsBusiness JobsMarketing JobsMarket Research Specialist JobsInternship Real World Evidence Rwe Jobs

Internship Real World Evidence Rwe information

See salary details

$8

$15

$21

How much do internship real world evidence rwe jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for internship real world evidence rwe in the United States is $15.54, according to ZipRecruiter salary data. Most workers in this role earn between $12.50 and $17.55 per hour, depending on experience, location, and employer.

What is an internship in real world evidence (RWE)?

An Internship in Real World Evidence (RWE) offers students or recent graduates hands-on experience in collecting and analyzing data from real-world sources, such as electronic health records, insurance claims, and patient registries. RWE is used in the pharmaceutical and healthcare industries to evaluate the effectiveness, safety, and value of medical treatments outside controlled clinical trials. Interns may support research studies, help interpret data, and contribute to reports that inform decision-making for healthcare providers and regulators. This type of internship is ideal for those interested in data analysis, public health, and evidence-based medicine.

What types of projects do interns typically work on in a real world evidence (RWE) internship?

As an RWE intern, you can expect to contribute to projects involving the collection, analysis, and interpretation of real-world healthcare data, such as electronic health records, claims data, or patient registries. Common responsibilities include supporting data cleaning, conducting literature reviews, assisting with statistical analyses, and preparing reports or presentations for internal teams. You will often collaborate with cross-functional teams including epidemiologists, data scientists, and medical affairs professionals, which provides excellent exposure to various aspects of the pharmaceutical or healthcare industry.

What are the key skills and qualifications needed to thrive as an internship real world evidence (RWE) professional?

To thrive as an Internship Real World Evidence (RWE) professional, you need a solid background in life sciences, epidemiology, or statistics, often supported by progress toward a relevant degree. Familiarity with data analysis tools like SAS, R, or Python, and experience with healthcare databases or real-world data systems, are typically required. Strong analytical thinking, attention to detail, and collaborative communication skills help interns excel in cross-functional teams and data-driven projects. These competencies are crucial for generating robust, actionable insights from real-world data to inform healthcare decisions and policy.

What is the difference between Internship Real World Evidence Rwe vs Data Analyst?

AspectInternship Real World Evidence RweData Analyst
Required CredentialsTypically pursuing or recent graduate in healthcare, life sciences, or related fieldsBachelor's degree in statistics, mathematics, computer science, or related fields
Work EnvironmentHealthcare or pharmaceutical companies, research organizations, or academic institutionsVarious industries including finance, healthcare, marketing, and technology
Employer & Industry UsageUsed in pharmaceutical, biotech, and healthcare sectors for evidence generationWidely used across multiple industries for data analysis and reporting

While both roles involve working with data, an Internship Real World Evidence Rwe focuses on analyzing real-world healthcare data to generate evidence for medical decisions, often within healthcare or pharma settings. A Data Analyst has a broader scope, working with various data types across industries to interpret and visualize data for business insights.

More about Internship Real World Evidence Rwe jobs

What cities are hiring for Internship Real World Evidence Rwe jobs?

Cities with the most Internship Real World Evidence Rwe job openings:

What are the most commonly searched types of Real World Evidence Rwe jobs?

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

What states have the most Internship Real World Evidence Rwe jobs?

States with the most job openings for Internship Real World Evidence Rwe jobs include:

What job categories do people searching Internship Real World Evidence Rwe jobs look for?

The top searched job categories for Internship Real World Evidence Rwe jobs are:

Internship Real World Evidence Rwe jobs near you
Infographic showing various Internship Real World Evidence Rwe job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 20% Part Time, 3% Contract, and 1% Nights. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $32,333 per year, or $15.5 per hour.

Associate Director, Real World Evidence (RWE) Science

Ubertal Inc

Waltham, MA • Remote

Contractor

Re-posted 3 days ago

Job description

Job Title: Associate Director, Real World Evidence (RWE) Science – Phase IV / Post-Approval (Contract)

Location: United States (Remote; Eastern Time business hours preferred)
Duration: 7-Month Contract (Full-Time, 40 hours/week)
Start: Targeting Early March 2026

We are seeking an experienced Associate Director, Real World Evidence (RWE) Science to provide coverage for a Phase IV / post-approval RWE portfolio within a global Medical Affairs environment. This is a senior-level individual contributor role requiring deep epidemiology and real-world evidence expertise, strong methodological leadership, and the ability to independently manage ongoing studies with minimal ramp-up.

This position supports global stakeholders, including Europe, and requires flexibility for early morning meetings aligned to EU collaboration.

Key Responsibilities

  • Lead scientific oversight of Phase IV and post-approval real-world evidence (RWE) and observational studies

  • Provide methodological and technical leadership for study design, feasibility assessments, and evidence planning (EU focus)

  • Oversee vendors/CROs conducting outsourced analyses; review protocols, statistical analysis plans, and outputs to ensure scientific rigor

  • Conduct and/or supervise systematic literature reviews (SLRs) and meta-analyses

  • Contribute to development of RWE plans aligned with regulatory, HTA, and post-approval commitments

  • Support retrospective analyses leveraging real-world data sources (claims, EHR, registries)

  • Guide protocol development for observational studies and pragmatic trials

  • Perform evidence reviews to inform regulatory submissions, reimbursement strategy, and medical strategy

  • Collaborate with Regional Medical Affairs on scientific exchange and external RWE engagement

  • Support development of abstracts, posters, manuscripts, and internal scientific communications

Required Qualifications

  • Advanced degree (MD, PhD, or MS) in Epidemiology, Biostatistics, Public Health, or related field

  • 8–10+ years of progressive experience in epidemiology and real-world evidence

  • Minimum 5 years of Pharma or Biotech industry experience

  • Strong expertise in:

    • Phase IV / post-approval epidemiologic study design

    • Retrospective real-world data (RWD) analyses

    • Observational research methodologies

  • Experience overseeing vendors/CROs and critically evaluating statistical methodologies

  • Proficiency with statistical software (R, SAS, Stata) and strong understanding of claims/EHR data structures

  • Demonstrated ability to work autonomously in a global, matrixed environment

  • Flexibility to support EU collaboration across time zones

Preferred Qualifications

  • Experience supporting regulatory or HTA-facing RWE deliverables

  • Vaccines, infectious disease, or public health epidemiology background

  • Experience with systematic literature reviews and meta-analyses

  • R programming skills, including simulations, power calculations, or Shiny applications

  • Experience with data extraction, cleaning, and standardization for RWD

  • Prior authorship of scientific publications and presentations

  • Experience supporting EU feasibility assessments and RWE expectations

Role Highlights

  • Senior-level RWE leadership without people management responsibilities

  • High-visibility Phase IV and real-world effectiveness portfolio

  • Global collaboration with strong EU engagement

  • Remote flexibility within the United States

Qualified candidates with deep RWE and epidemiology expertise, strong methodological grounding, and Phase IV experience in Pharma/Biotech are encouraged to apply.