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Real World Evidence Intern Jobs in Illinois (NOW HIRING)

Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real ... As a AI Data Science Intern, you will: * Design and implement advanced machine learning models and ...

About the Role The Key Account Director will own and expand strategic partnerships with MedTech, Pharma, and industry partners engaged in Real-World Evidence (RWE) and data-driven initiatives. You'll ...

Client Solutions Director

Chicago, IL · On-site

$170K - $220K/yr

A key area of focus will be supporting pilot programs related to Precision Patient Identification (PPI) and other terminology-driven solutions supporting clinical research, real-world evidence, and ...

Client Solutions Director

Rosemont, IL · On-site

$170K - $220K/yr

A key area of focus will be supporting pilot programs related to Precision Patient Identification (PPI) and other terminology-driven solutions supporting clinical research, real-world evidence, and ...

Client Solutions Director

Chicago, IL · On-site +1

$170K - $220K/yr

A key area of focus will be supporting pilot programs related to Precision Patient Identification (PPI) and other terminology-driven solutions supporting clinical research, real-world evidence, and ...

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Real World Evidence Intern information

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.

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 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 are the most commonly searched types of Real World Evidence jobs in Illinois? The most popular types of Real World Evidence jobs in Illinois are:
What job categories do people searching Real World Evidence Intern jobs in Illinois look for? The top searched job categories for Real World Evidence Intern jobs in Illinois are:
What cities in Illinois are hiring for Real World Evidence Intern jobs? Cities in Illinois with the most Real World Evidence Intern job openings:
Scientific Director, Clinical and Real World Evidence

Scientific Director, Clinical and Real World Evidence

AbbVie

North Chicago, IL • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 4 days ago


AbbVie rating

8.8

Company rating: 8.8 out of 10

Based on 95 frontline employees who took The Breakroom Quiz

11th of 70 rated pharmaceutical


Job description

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

Job Description:

The Quantitative Insights Lab (QuIL) within the Quantitative Medicine and Genomics organization at AbbVie is seeking a Scientific Director who will lead clinical and real world evidence (RWE) strategy, execution, and innovation within AbbVie's Quantitative Insights Lab (QuIL). This role is both a hands-on scientific contributor and a team leader, driving integration of complex human data-including multi-omics-with clinical, EHR and biobank health datasets. This position is critical for generating integrated evidence that directly informs the R&D pipeline decisions, ensuring scientific and clinical impact across AbbVie's therapeutic areas. The incumbent will design and implement robust studies, foster data-driven decision-making through advanced analytics and AI, and advance translational research in a highly matrixed and agile environment.

Key Responsibilities:

  • Serve as scientific and technical lead for clinical and real-world evidence initiatives, contributing subject matter expertise to organizational strategy, project design, and execution.
  • Lead and enable agile, cross-functional teams for integrated data projects to inform pipeline and strategic decisions, acting as either/both an individual scientific contributor and project leader
  • Oversee the curation, design and analysis of patient cohorts that leverage clinical, multi-omic, EHR, biobank phenotypic and real-world data to generate actionable insights for drug discovery, biomarker identification, and patient stratification.
  • Collaborate closely across functions-including other RWD teams-to harmonize data workflows and methodologies and align evidence generation with pipeline needs.
  • Communicate findings and strategy effectively to internal leadership, external collaborators, and cross-functional partners.
  • Stay abreast of latest methodologies and best practices for real world data, EHR analytics, multi-omic data integration, and related AI-driven approaches.
  • Play a key role as a member of the QuIL leadership team, helping to shape QuIL's strategic direction and supporting broader organizational initiatives.
Qualifications

Required Qualifications:

  • M.D. degree is required; board certification and clinical expertise strongly preferred.
  • At least 4 years of hands-on experience in real world evidence (RWE), electronic health record (EHR) analytics, ideally within the pharmaceutical, biotechnology, or academic research environment.
  • Demonstrated track record in designing and leading interdisciplinary clinical data science initiatives, including both hands-on scientific contribution and project management.
  • Advanced knowledge of data integration strategies and analytical methodologies for combining clinical, genomic, and real world data sources.
  • Excellent communication skills, with experience presenting scientific findings to internal and external stakeholders.
  • Familiarity in key analytics tools/languages (e.g., R, Python, SQL) is preferred but not necessary.
  • Familiarity with regulatory guidance and considerations for RWE and integrated evidence generation.

Preferred Qualifications:

  • Previous industry experience in pharmaceutical or biotechnology companies working with large-scale biobank and/or EHR datasets.
  • Strong track record of relevant scientific publications and presentations.
  • Demonstrated experience in aligning data science strategies with R&D pipeline objectives and measurable business outcomes
Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: 

  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at thetime of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location,and we may ultimately pay more or less than the posted range. This range may be modified in the future. 

  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.

  • This job is eligible to participate in our short-term incentive programs. 

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of anybonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's soleand absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law. 

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html


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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013