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Internship Real World Evidence Rwe Jobs in Pennsylvania

Jj

Director HTA Statistics & RWE Methods

Horsham, PA · On-site

$164 - $282.90/hr

... real-world evidence (RWE). The role spans all therapeutic areas and supports key innovative medicines across the lifecycle, from early development through launch and post-launch. Major Duties ...

PurpleLab Inc

Account Executive, Life Sciences

Wayne, PA · On-site

$150K - $185K/yr

You will position PurpleLab's powerful healthcare data analytics platform to support client initiatives across commercial strategy, real world evidence (RWE), and market access. This is a high-impact ...

Neurocrine Biosciences

Biostatistics Director

Indiana, PA · On-site

$130 - $180/hr

... of real world evidence (RWE) strategies, protocol development, analysis plan development, implementation of analyses, interpretation of findings and dissemination/publications. Ensures scientific ...

COMPASS Pathways

HEOR Science Liaison

Philadelphia, PA · 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 ...

ICON

Senior Account Executive

Blue Bell, PA · On-site

Experience selling Real-World Evidence (RWE) preferred. * Strong understanding of clinical trial operations, regulatory requirements, and industry standards. * Excellent communication, negotiation ...

Icon plc

Senior Account Executive

Blue Bell, PA · Remote

Experience selling Real-World Evidence (RWE) preferred. * Strong understanding of clinical trial operations, regulatory requirements, and industry standards. * Excellent communication, negotiation ...

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Internship Real World Evidence Rwe information

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.

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

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

What are popular job titles related to Internship Real World Evidence Rwe jobs in Pennsylvania?

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

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

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

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

Internship Real World Evidence Rwe jobs near you
Infographic showing various Internship Real World Evidence Rwe job openings in Pennsylvania as of August 2026, with employment types broken down into 1% As Needed, 72% Full Time, 24% Part Time, 2% Contract, and 1% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution.

Senior Director, Head of Medical Evidence Generation

CSL

King Of Prussia, PA • On-site

$303K - $371K/yr

Full-time

Re-posted 20 days ago

Job description

Position Summary

The Senior Director, Head of Medical Evidence reports into the Vice President, Head of Disease Areas and coordinates with Medical Affairs and cross-functional stakeholders to lead the Integrated Evidence Generation Plans (IEGP) for all marketed products and oversees the design and implementation of Medical Affairs evidence generation projects in alignment with GxP and business strategy.

Main Responsibilities and Accountabilities

  • Responsible for oversight and delivery of the strategic integrated evidence generation plans (IEGPs) across therapeutic areas for pipeline and marketed medicines. This includes development, execution, and maintenance of data gap generation and analysis and governance and documentation of all IEGPs.

  • Oversee design and implementation of Medical Affairs-led real-world evidence (RWE), epidemiological studies, HEOR, patient preference, and non-interventional studies. Guide development of phase IIIb/IV trials, registries, and observational studies. Ensure quality and timely delivery of study protocols, statistical analysis plans, and reports.

  • Anticipate evidence gaps and proactively adjust tactical plans to serve the data needs of key stakeholders, including Regulatory authorities, HTAs, HCPs, and payers.

  • Ensure all activities comply with GCP, regulatory standards, and internal policies. Manage budgets, timelines, and vendor relationships. Monitor and report on the impact of evidence generation activities.

  • Oversees study tracking of all ongoing Medical Affairs evidence generation projects globally and provides regular reporting to Medical Affairs, including LT, MAST, DA leads.

  • Enhance Medical Affairs capabilities in lifecycle management and phase 3b evidence generation.

  • Partner with Global Program Teams, Medical Affairs, Clinical Development, Regulatory, and Market Access. Lead or contribute to matrix teams and evidence generation sub-teams. Provides subject matter expertise and consultation to Medical Affairs colleagues in study development and design and interact, as required, with external research partners including investigators and vendors (including but not limited to CROs, database owners, registries, et). Provide support to Medical Disease Area teams for study execution as required.

Qualifications

Education:

  • Advanced degree (MS/PhD/PharmD) with relevant scientific/medical background

Experience:

  • Minimum of 12 years in pharmaceutical/biopharmaceutical industry inclusive of Medical Affairs.

  • 8+ years’ experience in research related experience and/or pharmaceutical industry experience.

  • Experience with late-stage clinical studies, research collaborations and RWE Proven track record of strong leadership, project management and demonstrated ability to coach and mentor individuals.

  • Strong Regulatory and medical information communications knowledge and experience.

  • Ability to communicate and interact thoughtfully, transparently, and appropriately with a variety of stakeholders both internal and external.

  • Experience building and leading cross-functional team in a global matrix organization.

Competencies:

  • Analytical thinking

  • Business acumen

  • Customer focus

  • Communication clarity

  • Emotional Intelligence (EQ)

  • Perseverance

  • Presentation expertise

  • Priority setting

  • Scientific expertise

The expected base salary range for this position at hiring is $303,000 - $371,000. Please note this salary range reflects the minimum and maximum base pay that CSL expects to pay for this position in Waltham, MA as of the time of this posting. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity.

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Commonwealth Serum Laboratories logo

About Commonwealth Serum Laboratories

Sourced by ZipRecruiter

Commonwealth Serum Laboratories (CSL) is a global leader in biotechnology, based in King of Prussia, Pennsylvania. The company originates from Australia, founded in 1916 by the Australian government to service the country’s health needs. Since then, CSL has expanded operations to become a multinational specialty biotechnology company that researches, develops, and manufactures vaccines and plasma protein biotherapies. Their mission is underpinned by focused, patient-driven values. Our commitment to saving lives and protecting people's health by providing safe and effective products is a testament to the difference we are making. One of their considerate achievements includes establishing one of the largest influenza vaccine providers in the world through their brand Seqirus.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

King of Prussia, PA, US

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