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Real World Evidence Rwe Jobs in Georgia (NOW HIRING)

Clinical Value Liaison

Atlanta, GA ยท On-site

$235K - $246K/yr

... real-world evidence (RWE), health economics and outcomes research (HEOR), and value-based care. The role generates actionable insights that inform Medical Affairs strategy while helping address ...

... data management, and real-world evidence functions with reliable, compliant, and scalable ... RWE workloads. Manage configuration, patching, upgrades, and troubleshooting for Axway Secure ...

... RWE workloads. Manage configuration, patching, upgrades, and troubleshooting for Axway Secure ... data management, and real-world evidence functions with reliable, compliant, and scalable ...

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 ...

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 ...

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

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

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

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

What job categories do people searching Real World Evidence Rwe jobs in Georgia look for?

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

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

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

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

Senior Real World Evidence Expert (United States)

Atlanta, GA โ€ข On-site

UCB
Finance and Insuranceย โ€ขย 1 - 5K employees

Full-time

Posted 11 days ago


Job description

Make your mark for patients
We are looking for a Senior Real World Evidence Expert who is scientifically rigorous, strategically minded, and collaborative to join our Real-World Evidence (RWE) team, helping to shape evidence generation strategies that support better decisions for patients, healthcare systems, and the broader scientific community. This position can be based in Brussels, Belgium; Slough, UK; Monheim, Germany or Atlanta, USA.
About the Role As Senior RWE Expert, you will be responsible for designing and delivering global real-world evidence (RWE) studies that generate impactful insights across the product lifecycle. You will contribute to strategic decision-making by developing evidence that supports research and development activities, regulatory requirements, payer needs, and clinical practice.
In this role, you will help drive the development of asset-level RWE strategies, working closely with cross-functional stakeholders to identify evidence gaps, generate meaningful insights, and advance innovative approaches to evidence generation. You will also contribute to the evolution of real-world data capabilities and methodologies that strengthen UCB's ability to address complex healthcare challenges.
Who You'll Work With You will work closely with RWE Strategy Leads, Epidemiology and Evidence Synthesis teams, Safety and Pharmacovigilance colleagues, Biostatisticians, Data Scientists, and external research partners. You will collaborate across global functions to ensure evidence generation activities are aligned with strategic priorities and deliver meaningful value to patients and stakeholders.
What You'll Do
  • Lead the design, execution, and delivery of complex global RWE studies on time and within budget.
  • Develop study concepts, protocols, statistical analysis plans, and study documentation to support evidence generation objectives.
  • Drive epidemiology, natural history, disease burden, comparative effectiveness, safety, and post-launch evidence generation initiatives.
  • Lead secondary data studies and represent RWE in primary data collection study teams.
  • Collaborate with external vendors, academic researchers, and medical experts to ensure high-quality study execution.
  • Interpret and communicate study findings to both internal and external stakeholders.
  • Support the development and execution of asset-level RWE strategies and evidence plans.
  • Identify and implement innovative study designs, advanced analytics methodologies, and new real-world data sources.
  • Contribute to scientific publications, abstracts, posters, presentations, and external communications.
  • Act as a trusted subject matter expert, providing strategic guidance and championing scientifically robust methodologies.

Interested? For this role we're looking for:
  • Master's degree, PhD, MD, or equivalent qualification in epidemiology, outcomes research, health economics, biostatistics, life sciences, or a related discipline.
  • Significant experience designing and delivering real-world evidence studies using primary and/or secondary data sources.
  • Strong expertise in epidemiology, pharmacoepidemiology, outcomes research, health economics, biostatistics, data science, or related quantitative disciplines.
  • Experience working within pharmaceutical, biotechnology, consulting, or academic research environments.
  • Excellent communication skills with the ability to translate complex evidence into clear and actionable insights.
  • Passion for innovation, scientific excellence, and the application of emerging technologies, including AI-enabled approaches within real-world evidence generation.

Are you ready to 'go beyond' to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe, inspired by patients and driven by science.
Why work with us?
At UCB, we don't just complete tasks, we create value. We aren't afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We 'go beyond' to create value for our patients, and always with a human focus, whether that's on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.
At UCB, we've embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.
UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.