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Real World Evidence Rwe Jobs (NOW HIRING)

ZS

Medical & Evidence Manager

Boston, MA · On-site

This role will work directly within the Medical & Evidence Generation space, partnering closely with stakeholders across Drug Development, Clinical Operations, Real-World Evidence (RWE), Medical ...

Parexel

Senior RWE Programmer

Parexel is seeking a Senior Real-World Evidence, RWE Programmer Join a high-impact team as a remote Sr. Real-World Evidence Programmer , supporting innovative work. You can work remotely out of ...

Parexel

Parexel is seeking a Senior Real-World Evidence, RWE Programmer Join a high-impact team as a remote Sr. Real-World Evidence Programmer , supporting innovative work. You can work remotely out of ...

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Real World Evidence Rwe information

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 jobs are there in clinical trials?

Jobs in clinical trials include Clinical Research Coordinators, Clinical Data Managers, Clinical Research Associates, and Study Monitors. These roles involve tasks such as patient recruitment, data collection, monitoring trial progress, and ensuring compliance with regulations, often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications. The work environment is typically in hospitals, research centers, or pharmaceutical companies, with schedules varying from standard to flexible hours.

What is RCT and RWE?

In the context of a Real World Evidence (RWE) role, RCTs (Randomized Controlled Trials) are clinical studies that randomly assign participants to different treatments to assess efficacy, while RWE involves analyzing data from real-world settings like electronic health records and insurance claims to evaluate treatment effectiveness outside controlled trials. Both are important for informing healthcare decisions and regulatory approvals, with RWE complementing RCT data by providing insights from everyday clinical practice.

What is Real World Evidence (RWE) in the healthcare industry?

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.

What are the roles in clinical trials?

In clinical trials, roles include Principal Investigator who oversees the study, Study Coordinators who manage daily operations, Data Managers who handle data collection and analysis, and Regulatory Affairs Specialists who ensure compliance with regulations. These roles require specific skills, certifications, and knowledge of Good Clinical Practice (GCP) guidelines to ensure the trial's integrity and participant safety.

What are the key skills and qualifications needed to thrive as a Real World Evidence (RWE) professional, and why are they important?

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.

How does a Real World Evidence (RWE) professional typically collaborate with cross-functional teams in the pharmaceutical industry?

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 is RWE in clinical research?

Real World Evidence (RWE) in clinical research refers to data collected from real-world settings outside controlled clinical trials, such as electronic health records, insurance claims, and patient registries. RWE helps researchers and healthcare professionals understand how treatments perform in routine practice and supports decision-making for drug development and regulatory approval.
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Real World Evidence Rwe jobs near you
Infographic showing various Real World Evidence Rwe job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, and 2% Contract. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution.
Head of Software - Real World Evidence - USA

Head of Software - Real World Evidence - USA

6AM City, LLC

Manhattan, NY • On-site

$150 - $180/hr

Other

Posted 23 hours ago

Job description

Job Description

Luminary Group is seeking an experienced and visionary Head of Software to lead our client's software development efforts in the field of Real World Evidence (RWE). As the Head of Software, you will be responsible for driving the technical direction, strategy, and execution of high-quality software solutions that leverage RWE data to drive insights and decision-making in the healthcare industry.

Responsibilities
  • Lead and manage a team of software engineers, providing technical guidance, mentorship, and performance feedback.
  • Define and execute the software development strategy and roadmap, aligning with the company's overall goals and objectives.
  • Collaborate with cross-functional teams to understand business requirements and translate them into technical solutions.
  • Oversee the design, development, and maintenance of software applications and systems that leverage RWE data.
  • Ensure the quality, scalability, and performance of software solutions through effective development practices and testing methodologies.
  • Stay updated on emerging technologies and industry best practices, and drive their adoption within the organization.
  • Prioritize and manage software development projects, ensuring timely and successful delivery.
  • Establish and enforce software development standards, documentation, and coding best practices.
  • Collaborate with stakeholders to troubleshoot and resolve technical issues and challenges.
  • Manage relationships with vendors, partners, and external service providers to ensure seamless integration and delivery of software solutions.
  • Stay abreast of industry trends and regulatory changes related to software development and RWE.
Requirements
  • Bachelor's degree in computer science, engineering, or a related field; advanced degree preferred.
  • Minimum of 8 years of experience in software development, with a focus on developing solutions in the healthcare industry.
  • Proven track record of leading and managing software engineering teams in agile development environments.
  • Strong knowledge of software development methodologies, technologies, and best practices.
  • Experience with RWE data and familiarity with healthcare data standards.
  • Proficiency in programming languages such as Java, C#, or Python.
  • Experience with web application development frameworks and technologies (e.g., Angular, React, Node.js).
  • Experience with cloud-based platforms and services (e.g., AWS, Azure) is preferred.
  • Strong analytical and problem-solving skills, with the ability to find creative solutions to complex technical challenges.
  • Excellent communication and leadership skills, with the ability to effectively collaborate with both technical and non-technical stakeholders.
  • Ability to thrive in a fast-paced, dynamic environment and effectively manage competing priorities.
  • Experience in the healthcare industry and knowledge of regulatory considerations in software development is a MUST.
  • Authorization to work in the United States.
  • Willingness to travel as required.
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