Parexel
Healthcare Insurance • Biotechnology • Pharmaceuticals
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.
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
đź’Š Pharmaceuticals
đź’° Venture Round on 1990-01
Statistical Programmer II
November 17
Parexel
Healthcare Insurance • Biotechnology • Pharmaceuticals
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.
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
đź’Š Pharmaceuticals
đź’° Venture Round on 1990-01
đź“‹ Description
• Provide technical expertise for the conduct of clinical trials • Work with minimal supervision to support various programming activities related to the analysis and reporting of clinical study data • Specialize in one of the following therapeutic area: hematology/oncology/cell therapy • Use SAS programming to produce derived datasets (ADaM), tables, figures, and data listings of varying complexity • Develop and QC derived dataset specifications and other process supporting documents • Ensure all work maintains complete traceability and regulatory compliance • Participate and contribute to knowledge-sharing sessions with programming community
🎯 Requirements
• Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences • Minimum 3 years of SAS programming experience in clinical research • Proficiency in SAS Base, SAS/STAT, SAS/GRAPH, and SAS macros • Strong understanding of CDISC standards • Knowledge of statistical terminology, clinical tests, and protocol designs • Excellent attention to detail with a focus on quality • Strong written and verbal English communication skills
🏖️ Benefits
• Fully flexible work arrangement • Opportunity to develop within your role • Open and friendly work environment
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