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Real World Evidence Rwe Jobs in Acworth, GA (NOW HIRING)

Who you will work with You will collaborate across Development, Medical, Real-World Evidence, Commercial, Integrated Insights, the Global Data Office, and Digital Technology teams. Partnerships with ...

Who you will work with You will collaborate across Development, Medical, Real-World Evidence, Commercial, Integrated Insights, the Global Data Office, and Digital Technology teams. Partnerships with ...

Senior Scientist R&D

Atlanta, GA · On-site

$94K - $135K/yr

Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for ...

Who you'll work with You will co-create with Integrated Insights Leads from early asset and late stage (Phase 0-3) teams , Real world evidence teams, Translational Medicine and Bioinformatics ...

Who you'll work with You will co-create with Integrated Insights Leads from early asset and late stage (Phase 0-3) teams , Real world evidence teams, Translational Medicine and Bioinformatics ...

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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 cities near Acworth, GA are hiring for Real World Evidence Rwe jobs? Cities near Acworth, GA with the most Real World Evidence Rwe job openings:
Associate Director, Health IT

Associate Director, Health IT

Taylor Strategy Partners

Atlanta, GA • On-site

$140K - $180K/yr

Full-time

Medical, Dental, Vision, Retirement

Posted 7 days ago


Job description

Description
About Arrowhead Pharmaceuticals
Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) develops medicines that treat intractable diseases by silencing the genes that cause them. Using RNAi-based technologies, Arrowhead is pioneering therapies with rapid, deep, and durable target gene knockdown. Our clinical pipeline includes promising therapies for rare cardiometabolic conditions such as Familial Chylomicronemia Syndrome (FCS) and Severe Hypertriglyceridemia (SHTG). Arrowhead is headquartered in Pasadena, CA with research and development facilities in Madison, WI and San Diego, CA.
The Position
Arrowhead Pharmaceuticals is seeking an Associate Director to focus on identifying unmet needs and gaps in care across health systems for patients with rare cardiovascular diseases. This role emphasizes understanding how health information technologies and real-world evidence can help close care gaps, improve patient identification, and drive better outcomes. By collaborating with healthcare providers, decision-makers, and internal Arrowhead teams, this individual will highlight opportunities where EHR optimization can shape care delivery.
Responsibilities
Identify Gaps in Care
  • Partner with health systems to understand unmet needs in rare cardiovascular disease management.
  • Assess where patients are missed or underdiagnosed and highlight barriers to care delivery.

Generate Insights & Evidence
  • Collect real-world insights on system challenges, patient pathways, and access barriers.

Support System Engagement
  • Facilitate dialogue with clinical, IT, and administrative leaders to uncover opportunities for better patient identification and care coordination.
  • Communicate how health IT tools and real-world data can be leveraged to address gaps in diagnosis and treatment.

Collaborate Across Functions
  • Share insights with Market Access, Medical Affairs, and Commercial teams to guide resource development and strategy.
  • Ensure findings align with compliance and regulatory standards.

Experience
  • Bachelor's degree required; advanced degree (MS, MPH, PharmD, PhD, or equivalent) preferred.
  • 5+ years' experience in health economics, outcomes research, medical affairs, or related healthcare field.
  • Experience working with health systems, payers, or research teams to identify gaps in care and assess value.

Skills & Competencies
  • Strong understanding of EHR capabilities across different platforms.
  • Ability to synthesize real-world insights and communicate value narratives.
  • Excellent stakeholder engagement, communication, and analytical skills.
  • Familiarity with real-world evidence generation and health system trends is beneficial.

Success Metrics
  • Identification of key gaps in patient care pathways.
  • Quality and relevance of real-world insights gathered from health systems.
  • Impact on EHR pathways and workflows.
  • Contribution to improved patient identification and evidence-based adoption of therapies.

Compensation & Benefits
  • Competitive base salary: $140,000-$180,000, plus incentive compensation.
  • Equity (RSUs) and car allowance program.
  • Comprehensive benefits package: health, dental, vision, 401(k).

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