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Real World Evidence Rwe Jobs in Florida (NOW HIRING)

Experience in post-market, real world evidence, longitudinal or health economics studies is preferred. * Ability to generate and develop ideas that drive efficiency and impact organizational goals.

Experience in post-market, real world evidence, longitudinal or health economics studies is preferred. * Ability to generate and develop ideas that drive efficiency and impact organizational goals.

We move quickly, validate assumptions with evidence, and simplify aggressively to deliver systems ... Scientific Rigor and Real-World Impact * Leadership and Growth * Collaborative Culture

... and real-world experiences necessary to excel in college or career pathways. KIPP Miami Tech will ... You use evidence to refine instruction and accelerate student growth. * Heartbeat Aligned: You ...

Bioinformatics Scientist

Winter Park, FL · On-site

$150K - $180K/yr

Hunt down bugs and tame the chaos of real-world sequencing data, including biological artifacts and ... Proven experience building scalable bioinformatics products and clear evidence of delivering ...

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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.
What are the most commonly searched types of Real World Evidence Rwe jobs in Florida? The most popular types of Real World Evidence Rwe jobs in Florida are:
What cities in Florida are hiring for Real World Evidence Rwe jobs? Cities in Florida with the most Real World Evidence Rwe job openings:
Infographic showing various Real World Evidence Rwe job openings in Florida as of July 2026, with employment types broken down into 69% Full Time, and 31% Part Time. Highlights an 72% In-person, 14% Hybrid, and 14% Remote job distribution.
Knees and Spine HEMA Analyst

Knees and Spine HEMA Analyst

Johnson & Johnson

Palm Beach Gardens, FL • On-site

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.


Johnson & Johnson rating

8.2

Company rating: 8.2 out of 10

Based on 108 frontline employees who took The Breakroom Quiz

29th of 73 rated pharmaceutical


Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Market Access

Job Sub Function:

Health Economics Market Access

Job Category:

Professional

All Job Posting Locations:

Palm Beach Gardens, Florida, United States of America, Raritan, New Jersey, United States of America, Raynham, Massachusetts, United States of America, Toronto, Ontario, Canada, Warsaw, Indiana, United States of America, West Chester, Pennsylvania, United States of America

Job Description:

Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.

DePuy Synthes is recruiting for a Knees and Spine HEMA Analyst located in West Chester PA, Raynham MA, Raritan NJ, Warsaw IN, Palm Beach Gardens FL, or Toronto ON Canada.

Key Responsibilities

Evidence Generation & Literature Research

  • Conduct literature reviews, systematic reviews, and meta-analyses to support health economic and clinical evidence development for knee, spine, and digital surgery products

  • Perform targeted evidence searches to support competitive intelligence, product positioning, and payer engagement

  • Maintain and update evidence libraries, reference databases, and bibliographic files for the Knees and Spine portfolios

  • Summarize and critically appraise published clinical and economic evidence,identifyingkey findings and implications for HEMA strategy

  • Participate in the development of protocol-driven RWE studies

Health Economic Modeling & Analysis

  • Assistin the development and maintenance of health economic models, including cost-effectiveness and budget impact for knee replacement, spinal fusion, robotic-assisted surgery, and related procedures

  • Gather andvalidatemodel inputs from published literature, clinical data, claims analyses, and internal data sources

  • Conduct sensitivity analyses and scenario modeling to test assumptions and support decision-making

  • Analyze clinical trial data, registry data, and real-world evidence to generate insights for internal and external stakeholders

Value Communication & Deliverable Development

  • Support the creation of value briefs, evidence summaries, and stakeholder communication materials

  • Prepare data summaries, slide decks, infographics, and reports for cross-functional teams, advisory boards, and congress presentations

  • Assist with HTA submissions, ensuring accuracy and completeness of all supporting data

  • Develop andmaintainstandardized templates for HEMA deliverables to ensure consistency across the portfolio

Market Monitoring & Cross-Functional Support

  • Monitor the competitive landscape, published literature, clinical guidelines, and payer policy developments relevant to the knee and spine markets

  • Track and summarize key congress presentations, competitor publications, and emerging evidence trends

  • Support cross-functional teams including Marketing, Medical Affairs, R&D, and Regulatory with evidence-based insights and data requests

Project Coordination & Documentation

  • Maintain organized project trackers, timelines, and documentation to ensure on-time delivery of HEMA projects

  • Participate in team meetings and professional development activities

Qualifications

  • Bachelor's or Master'sdegree (preferred) in Health Economics, Public Health, Epidemiology, Biostatistics, or related field

  • 2-4 years of experience in HEOR, health economics, or market access; internship or fellowship experience considered

  • Proficiencyin Excel; experience with SAS, R, Stata, or similar statistical tools preferred; familiarity with literature databases (PubMed, Embase)

  • Strong quantitative and critical thinking skills with attention to detail

  • Clear written and verbal communication skills; ability to synthesize complex information into concise deliverables

  • Interest in or familiarity with the orthopedic/MedTech space is a plus

Other:

Travel up to 20%

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.

#LI-Hybrid

#DePuySynthesCareers

Required Skills:

Preferred Skills:

Business Savvy, Coaching, Communication, Competitive Landscape Analysis, Cross-Functional Collaboration, Customer Intelligence, Go-to-Market Strategies, Health Economics, Health Intelligence, Market Knowledge, Market Opportunity Assessment, Organizing, Pricing Strategies, Problem Solving, Regulatory Compliance, Relationship Building, Strategic Thinking

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