
10,000+ employees
Founded 1983
đź’Ľ Consulting
🏥 Healthcare
📦 Logistics
đź’° Venture Round on 1990-01
Consulting • Healthcare • Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
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10,000+ employees
Founded 1983
đź’Ľ Consulting
🏥 Healthcare
📦 Logistics
đź’° Venture Round on 1990-01
Consulting • Healthcare • Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
• Effectively designs and codes R and SQL programs for assigned project(s) • Clean and validate RWD for consistency and reliability • Implement programming as specified from RWE protocol • Create or review and approve programming plans at study and project level • Maintain clear documentation of analytical programming and operational definitions • Develop dashboards, reports, and presentations to communicate findings • Collaborate with members of study teams to meet study and recurring report timelines
• MS in data science, epidemiology, statistics, public health, or related discipline • At least 2-3 years of experience in Real-World Data (RWD) analysis and Real-World Analytics (RWA) • Hands-on experience with Flatiron data required • Fluency in SQL and R programming is required • Experience writing original code and performing raw data analysis • Knowledge of SAS and/or Python is considered an advantage • Familiarity with US and global healthcare coding systems • Experience conducting routine and advanced statistical analyses for RWE generation • Deep understanding of observational study analysis • Strong communication and collaboration skills
• Health insurance • Professional development
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