Biostatistician II

🔥 0 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

⚕️ Healthcare Insurance

🧬 Biotechnology

💊 Pharmaceuticals

💰 Venture Round on 1990-01

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.

📋 Description

• Lead, advise and review: Leverage your expertise. Independently leads the development and execution of statistical aspects for studies of low to moderate complexity. • Develop complex analysis strategies and execute them using efficient programming techniques (software: SAS, R). • Perform intricate statistical analyses and provide input to statistical reports. • Share knowledge. Provide input to analysis plans, statistical reports, statistical sections of integrated clinical reports. • Be a proactive advisor for all types of analysis from the proposal process through the project life cycle. • Review analysis data sets and quality control all types of statistical analysis deliverables. • Liaise with biostatistical and other company departments to optimize global efficiency.

🎯 Requirements

• Master's Degree in Statistics (or equivalent) plus a minimum of 3 years industry experience OR PhD in Statistics (or equivalent) plus 1 year of industry related experience • A thorough understanding of the statistical aspects of clinical trials and/or observational studies • Experience in statistical analysis in a clinically related subject, within clinical trials • SAS programming or R programming skills (desired)

🏖️ Benefits

• Collaborate on global, cross-functional teams • Flexible working hours