Real World Evidence
Fortrea
Real World Evidence
Fortrea
Global CRO providing Phase I-IV trials
Job Overview:
The RWE SAS Programmer, CDISC/SDTM specs position is responsible for supporting our Real-world Evidence (RWE) services through successful delivery of complex analyses of data generated from global prospective and retrospective observational studies or existing secondary data sources (e.g., claims, hospital administration, electronic health records, registries). The Senior Associate, RWD Analyst follows analytic plans for data presentation under the guidance of our RWE biostatisticians and epidemiologists.
Summary of Responsibilities:
Client Delivery
Process Improvement
People
Business Development
Qualifications (Minimum Required):
Experience (Minimum Required):
Preferred Qualifications:
Physical Demands / Work Environment:
Learn more about our EEO & Accommodations request here.
Fortrea is a global contract research organization that provides clinical development services for the life sciences industry. It offers full service, functional service, and hybrid outsourcing models across Phase I–IV trials, clinical pharmacology, and consulting, serving biotech, biopharma, medical devices, and diagnostics. Its work is delivered through a network of investigators and specialized teams in approximately 100 countries, supporting trial design, execution, data management, and regulatory compliance. Fortrea’s approach combines its legacy experience from Covance and Labcorp with a pureplay CRO model to deliver fit-for-purpose solutions and agile project delivery. This positions it to manage trials across more than 20 therapeutic areas with scientific rigor and operational excellence. The company aims to bring predictability to clinical trial execution and help clients turn research ideas into real-world outcomes.
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