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Real World Evidence Rwe Jobs in Wayne, PA (NOW HIRING)

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The RWE Statistician is involved in planning, conducting and analyzing real-world evidence studies (prospective & retrospective observational study, electronic medical records, claim database ...

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Real World Evidence Rwe information

What is real world evidence (RWE)?

Real World Evidence (RWE) refers to clinical evidence regarding the usage and potential benefits or risks of a medical product, derived from analysis of real-world data (RWD). This data is collected from sources outside of traditional clinical trials, such as electronic health records, insurance claims, patient registries, and wearable devices. RWE plays a crucial role in understanding how treatments work in routine clinical practice, informing regulatory decisions, and supporting drug development and market access. Organizations use RWE to complement clinical trial data, improving healthcare outcomes and patient care.

How does a real world evidence (RWE) professional collaborate with cross-functional teams?

RWE professionals often work closely with colleagues from epidemiology, health economics, medical affairs, and regulatory affairs to design and execute studies using real-world data. Collaboration is essential, as RWE findings support evidence generation for regulatory submissions, market access, and post-marketing surveillance. Regular meetings, data-sharing sessions, and joint project planning are common, ensuring all stakeholders are aligned on study objectives, methodologies, and data interpretation. This collaborative environment helps translate complex data into actionable insights that support decision-making across the organization.

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

To thrive as a Real World Evidence (RWE) professional, you need a strong background in epidemiology, biostatistics, and data analysis, often supported by an advanced degree in a relevant scientific field. Familiarity with statistical software (such as SAS, R, or Python), real-world data sources (like EHRs and claims databases), and regulatory guidelines (FDA/EMA) is essential. Strong communication, problem-solving, and cross-functional collaboration skills help convey complex findings to stakeholders and integrate RWE into decision-making. These competencies are crucial for generating credible insights that inform clinical, regulatory, and commercial strategies in the healthcare industry.

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

AspectReal World Evidence RweClinical Data Analyst
Required credentialsTypically requires a background in healthcare, epidemiology, or biostatistics, often with a master's or PhDUsually requires a degree in health informatics, biostatistics, or related fields, with similar certifications
Work environmentPrimarily in healthcare, pharmaceutical, or research organizations analyzing real-world dataIn clinical research settings, hospitals, or pharmaceutical companies analyzing clinical trial data
Employer and industry usageUsed by pharma companies, healthcare providers, and research institutions to generate real-world insightsUsed by research organizations, hospitals, and pharma for clinical trial data management and analysis

Real World Evidence Rwe professionals focus on analyzing data from real-world settings like electronic health records and insurance claims, while Clinical Data Analysts primarily work with clinical trial data. Both roles require strong analytical skills and related credentials, but Rwe specialists emphasize real-world data sources to inform healthcare decisions.

What job categories do people searching Real World Evidence Rwe jobs in Wayne, PA look for?

The top searched job categories for Real World Evidence Rwe jobs in Wayne, PA are:

What cities near Wayne, PA are hiring for Real World Evidence Rwe jobs?

Cities near Wayne, PA with the most Real World Evidence Rwe job openings:

Infographic showing various Real World Evidence Rwe job openings in Wayne, PA as of August 2026, with employment types broken down into 50% Full Time, and 50% Part Time. Highlights an 100% In-person job distribution.

Remote Statistician-Real World Evidence (RWE)

King Of Prussia, PA • Remote

TechData Service Company LLC
Biotechnology Research and Development • 51 - 200 employees

$100K - $160K/yr

Contractor

Medical, Dental, Life, Retirement, PTO

Posted 12 days ago

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Job description

Purpose:

The RWE Statistician is involved in planning, conducting and analyzing real-world evidence studies (prospective & retrospective observational study, electronic medical records, claim database...), and/or large database .


The Statistician is responsible for working with research associates and scientists to establish a reporting database and for analyzing data for real world evidence studies.


Key Responsibilities:

The job tasks listed below outline the scope of the position. The application of these tasks may vary, based upon current business needs.


Study Design and Analysis

·        Operate in collaboration with scientist in design studies and write protocols for the conduct of research projects. 

·        Assist in or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the protocol and the statistical analysis plan, and conducting the actual analysis once a reporting database is created.

·        Collaborate with data sciences in the planning and implementation of data quality assurance plans. 

·        Maintain currency with respect to statistical methodology, maintain proficiency in applying new and varied methods, and to be competent in justifying methods selected.

·        Influence team members regarding appropriate research methods

·        Perform peer-review of work products from other statistical colleagues.

Communication of Results and Inferences

·        Collaborate with team members to write reports and communicate results. 

·        Assist with, or be responsible for, communicating study results via regulatory submissions, manuscripts, or oral presentations in group settings, as well as for communicating one-on-one with key customers and presenting at scientific meetings. 

·        Support responses to regulatory queries and/or regulatory interactions.


Therapeutic Area Knowledge

·        Understand disease states,  competitive landscapes, and regulatory environment in order to enhance the level of customer focus and collaboration and be seen as a strong scientific contributor.

Regulatory Compliance

·        Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable Corporate, Medical, local, and departmental policies, procedures, processes, and training.


Statistical leadership and Teamwork

·        Introduce and apply innovative methodology and tools to solve critical problems

·        Merge scientific thinking and business knowledge to identify issues, evaluate options and implement solutions.

Minimum Qualification Requirements:

§  Qualified Statistician (MSc, Ph.D). in Statistics OR Biostatistics with at least 3 years of experience in the pharmaceutical industry

§  Proven experience in conducting and analyzing real-world evidence studies (prospective & retrospective observational study, electronic medical records, claim database...), and/or large database

§  Prior experience in Rheumatology, Dermatology, or Gastroenterology would be an added value (but not mandatory)

Other Information/Additional Preferences:

·        Proficient in statistical programming languages/software such as SAS and/or R

·        Able to work in a virtual environment

·        Teamwork and leadership skills

·        Technical expertise and application with working knowledge of experimental design and statistical analysis

·        Self-management skills with a focus on results for timely and accurate completion of competing deliverables

·        Creativity and innovation

·        Demonstrated problem solving ability and critical thinking

Company Description

https://quantive.bio/