Principal Biostatistician

November 21

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Parexel

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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

💊 Pharmaceuticals

💰 Venture Round on 1990-01

📋 Description

• Provide broad statistical support, including trial design, protocol and CRF development on specific studies • Lead production and quality control of randomization, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents • Perform sample-size calculations, generate randomization lists and write statistical methodology sections for inclusion in study protocols • Provide statistical input into Data Monitoring Committee (DMC) activities, including development of DMC charters and analysis plans • Support business development by contributing to study design considerations in internal and client meetings • Understand regulatory requirements related to the specific therapeutic areas and the implications for statistical processing and analysis

🎯 Requirements

• PhD or MS in Statistics or related discipline • Prior experience with SAS programming • Competent in written and oral English in addition to local language • Thorough understanding of statistical issues in clinical trials • Ability to clearly describe advanced statistical techniques and interpret results • Familiarity with regulatory/research guidelines on drug development, GCP, and statistical principles (especially ICH guidelines)

🏖️ Benefits

• Health insurance • Retirement plans • Paid time off • Flexible work arrangements • Professional development