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Rwe Jobs in Georgia (NOW HIRING)

RWE

Manager, O&M

Carlton, GA · On-site

RWE Americas, LLC To start as soon as possible, full time, permanent Functional area: Operations & Maintenance Remuneration: Exempt the Manager, O&M is responsible for supervising the overall ...

RWE

Manager, O&M

Carlton, GA · On-site

RWE Americas, LLC To start as soon as possible, full time, permanent Functional area: Operations & Maintenance Remuneration: Exempt the Manager, O&M is responsible for supervising the overall ...

RWE Gruppe

Manager, O&M

Carlton, GA · On-site

$110 - $140/hr

RWE Americas, LLC To start as soon as possible, full time, permanent Functional area: Operations & Maintenance Remuneration: Exempt the Manager, O&M is responsible for supervising the overall ...

RWE AG

Manager, O&M

Carlton, GA · On-site

$90 - $130/hr

Create Alert RWE Americas, LLC To start as soon as possible, full time, permanent Functional area: Operations & Maintenance Remuneration: Exempt the Manager, O&M is responsible for supervising the ...

Syneos Health Careers

Clinical Value Liaison

Atlanta, GA · On-site

$235K - $246K/yr

Work with health care decision makers focused on payer initiatives, RWE, HEOR, and removing clinical and economic barriers to patient access. * Plan and execute strategy and engagement for assigned ...

CapTech Consulting

DevOps Engineer

Atlanta, GA · On-site

$50.75 - $69.50/hr

Additional Information RWe want everyone at CapTech to be able to envision a lasting and rewarding career here, which is why we offer a variety of career paths based on your skills and passions. You ...

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$76.3K

$125K

$179K

How much do rwe jobs pay per year?

As of Aug 23, 2026, the average yearly pay for rwe in Georgia is $125,036.00, according to ZipRecruiter salary data. Most workers in this role earn between $105,427.00 and $141,996.00 per year, depending on experience, location, and employer.

What is an RWE?

An RWE (Real-World Evidence) job involves analyzing real-world data from sources like electronic health records, claims databases, and patient registries to generate insights on treatment effectiveness, safety, and healthcare outcomes. Professionals in this field work in pharmaceuticals, healthcare, and regulatory organizations to support clinical decision-making and policy development. Their role includes data analysis, study design, and interpretation of findings to inform medical practice and drug development.

What are the primary day-to-day responsibilities of an RWE specialist?

As an RWE specialist, your daily tasks typically include designing and conducting observational studies using healthcare databases or patient registries, analyzing real-world data, and generating actionable insights for clinical or commercial teams. You may also collaborate closely with epidemiologists, medical writers, and regulatory affairs professionals to ensure the quality and compliance of research outputs. RWE specialists frequently present study results to both internal stakeholders and external partners, translating complex data into clear, actionable recommendations. The role offers the opportunity to work on diverse therapeutic areas and contribute valuable evidence supporting real-world patient outcomes.

What are the key skills and qualifications needed to thrive in the RWE position, and why are they important?

To thrive as a Real World Evidence (RWE) specialist, you need a solid background in epidemiology, biostatistics, and data analysis, typically supported by a relevant degree in life sciences or public health. Familiarity with data analysis software (such as SAS, R, or Python), database management systems, and knowledge of healthcare data standards are usually required. Critical thinking, attention to detail, and effective communication skills are vital soft skills for interpreting complex data and collaborating across multidisciplinary teams. These abilities are essential for accurately generating insights from real-world data to inform patient outcomes, regulatory decisions, and healthcare strategies.

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

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

What cities in Georgia are hiring for Rwe jobs?

Cities in Georgia with the most Rwe job openings:

Rwe jobs near you
Infographic showing various Rwe job openings in Georgia as of August 2026, with employment types broken down into 100% Full Time. Highlights an 50% Hybrid, and 50% Remote job distribution, with an average salary of $125,036 per year, or $60.1 per hour.

RWE Senior Expert - Special Patient Populations

UCB

Atlanta, GA • On-site

Full-time

Posted 5 days ago

Job description

Make your mark for patients
About the role:
As a Senior RWE Expert, you will be responsible for designing and executing global real-world evidence (RWE) projects that:
  • inform strategic internal decision-making thereby empowering differentiating R&D activities within UCB
  • support external decision making by key stakeholder groups such as patients, regulators, policy makers, payers, and prescribers
  • contribute to the wider epidemiological and medical understanding of specific diseases
  • develop the underlying real world data infrastructure for a specific disease / disease area related to women of childbearing age (WoCBA) and other special patient populations (SPP), including elderly and pediatrics.

You will drive the development of the overarching RWE Functional Strategic Plan for an asset in close collaboration with the Strategy lead for WoCBA/SPP.
What you'll do:
  • EXECUTION of RWE STUDIES on time and to budget:
  • input to / help drive the Global RWE Strategy & Tactical WoCBA/SPP Plan based on request from the RWE Strategy Lead responsible for the respective patient population/asset
  • E.g.: Epidemiology, Natural History/Burden, Care Pathways, Unmet Need; Gap analysis and new studies required for JCA; Background rates of safety outcomes; Regulatory studies including external control arms; Innovative hybrid study designs; Regulatory safety study commitments (PASS, PAES, PMS); Drug utilisation and early feedback post-launch; Comparative effectiveness including long term and patient centric outcomes; Data component of managed entry programmes / value-based contracts
  • writing study concept; writing study protocol; developing SAP; meeting quality control and governance requirements, reporting against milestones; consultation to local study teams; mitigation for operational issues
  • Leading Secondary Data Use Studies, including the most complex and high profile studies; and representing RWE on Primary Data Collection Study teams
  • Collaborating with external vendors and medical experts on RWE projects,
  • with BQS and RWE Analysts on the analysis plan
  • Lead the interpretation of results and communicating results internally and externally
  • Develop clearly defined evidence needs with
  • the Evidence Synthesis group for HE/HTA and value communication plans
  • Safety / Pharmacovigilance teams for regulatory needs
  • Supporting the RWE Strategy Lead to develop the overarching RWE Functional Strategic Plan for an asset
  • Provide strategic input to internal stakeholders based on RWE activities and robust epidemiological and medical understanding of WoCBA/SPP
  • Identifying opportunities for innovative study designs, use of new data sources and advanced analytic techniques to solve complex evidence generation problems
  • Consistently advocate for scientifically sound methods with internal and external stakeholders; being able to challenge and defend positions appropriately with a range of stakeholders

Interested? For this position you'll need the following education, experience and skills:
Minimum Qualifications:
  • Master's Degree
  • Experience successfully conceptualizing and delivering RWE projects using primary and secondary data (within the pharmaceutical industry or with a recognized expert consultancy or academic center of excellence)
  • 6 years of Global or regional experience
  • Excellent and effective oral/written skills in English

Preferred Qualifications:
  • PhD in epidemiology or outcome research with additional depth and breadth of experience
  • Ability to translate project work into scientific communications (e.g., abstracts, poster presentations, podium presentations, manuscripts)
  • Combination of strong methodological quantitative knowledge, strategic, innovative thinking, and communication skills
  • Experience in projects relating to fertility, preterm birth, obstetric illnesses, pregnancy, lactation and neonatal health AND/OR experience working with innovative RWE study designs and approaches
  • Interested in incorporating advanced analytics, machine learning, and AI into traditional RWD approaches
  • Background knowledge of industry trends and best practices, specifically related to epidemiology/outcomes research
  • Subject matter expert with strong quantitative methods skills including training in the areas of epidemiology, pharmacoepidemiology, outcomes research, health economics, biostatistics, data science or related disciplines
  • Ability to deliver impactful presentations to peers and/or internal stakeholders with a relaxed and proficient presentation style
  • Experience successfully working with multidisciplinary cross functional and cross-cultural project teams
  • Ability to use his/her relationships with internal and external stakeholder groups to provide strategic input through synthesized thinking, building advocacy and empowering implementation of the solutions in support of creating patient value and UCB portfolio performance
  • Passion for maternal and infant health
  • Passion for innovation and creativity. Able to learn fast and adapt to new ways of working, be open-minded and science driven.

This positions reasonably anticipated base salary range is $164,000 to $215,300 per year. The actual salary offered will take into account internal equity and may also vary depending on the candidate's geographic region, job-related knowledge, skills, and experience, among other factors.
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 explicitly 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 federal, state, or local law. UCB invites you to voluntarily self-identify during the application process. Provision of self-identification information is entirely voluntary and a decision to provide or not provide such information will not have any effect on your application for employment, your employment with UCB, or otherwise subject you to any adverse treatment. Any information you provide will be considered confidential and will be kept separate from your application and/or personnel file and will only be used in accordance with applicable laws, orders, and regulations.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on US-Reasonable_Accommodation@ucb.com for application to US based roles. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

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