As an experienced Real-World Data (RWD) Analyst in our Market Access Consulting & HEOR group supporting our Real-World Evidence (RWE) services, you are central to the successful delivery of complex analyses of data for reporting results of RWE studies, informing health economic models, and conducting post hoc analyses of clinical trial data.
In this role you will follow analytic plans for data presentation, prepare CDISC standard specifications and datasets, and provide SAS and/or R programming under the guidance of our RWE biostatisticians. Your work will have an impact on improving the health and lives of thousands of patients around the world.
The Senior Associate, RWD Analyst will support the analysis of data collected from global observational studies and will be primarily responsible for conducting analyses of primary and secondary data for formulating RWE.
Summary of Responsibilities:
- Provide programming support for the analysis of real-world data from diverse sources including prospective observational studies and retrospective data sources (eg, medical and pharmacy claims data, hospital data, electronic medical records).
- Help in contributing to the development of programming specifications based on analysis requirements and source data.
- Develop and validate analysis datasets from various file formats and sources, both internal and external.
- Assist in the development and validation of graphs and tables for exploratory investigations, adapting to changing analysis requirements.
- Ensure excellence in the programming of analysis-ready datasets, tables, figures, and listings, including associated validation work.
- Support the creation and maintenance of documentation for assigned deliverables.
- Assist in communicating accurate and timely status updates to project leads and team members.
- Participate in department meetings to share knowledge and insights.
- Assist in identifying opportunities to enhance productivity, quality, and efficiency in programming processes.
Qualifications (Minimum Required):
- Bachelor degree in statistics, mathematics, epidemiology, or other related field
- Proficiency in SAS programming
- Proficiency in CDISC standards (eg, SDTM specifications)
- Solid familiarity with R programming
- Ability to problem solve independently.
- Ability to follow defined processes.
- Strong oral and written communication.
- Working knowledge of Microsoft Word, PowerPoint and Excel.
Experience (Minimum Required):
- 2-3 years of analysis of real-world data in a contract research organization, health economics and outcomes research consulting practice, or pharmaceutical industry.
- Appling CDISC standards to observational data
- Programming SDTM, ADaM, and Tables/Figures/Listings (TFLs) using SAS and R programming languages
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
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What We Do
Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network.
Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.
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