Biostatistician II

Job not on LinkedIn

🔥 49 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 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.

📋 Description

• Contribute to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions • Independently program and quality-control derived datasets and statistical outputs, including tables, listings, and figures • Produce analysis plans and reports under the supervision of an experienced biostatistician • Provide basic statistical advice to clients • Produce and/or QC derived datasets and simple and advanced statistical outputs using efficient programming techniques • Understand and apply moderately advanced statistical methods • Coordinate and lead project teams to complete projects within timelines and budget • Interact with clients as a key contact regarding statistical and contractual issues • Assist with analysis plans, statistical reports, statistical sections of integrated clinical reports, and process-supporting documents • Check work on an ongoing basis to ensure first-time quality • Provide training in statistical analysis to internal clients • Participate in or lead process and quality improvement initiatives • Travel to, attend, and contribute to client meetings, including discussing analysis concepts and presenting study results

🎯 Requirements

• Master's Degree in Statistics plus a minimum of 3 years industry experience OR PhD in Statistics plus 1 year of industry related experience • 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 • Confidence, self-reliance, and ability to learn quickly in a matrixed team • Good leadership skills • Strong oral and written English communication skills • Strong work ethic to promote the development of life-changing treatments for patients

🏖️ Benefits

• Virtual resources supporting collaborative and effective work across the globe • Opportunities to work collaboratively with colleagues across the globe • Training in statistical analysis for internal clients • Participation in process and quality improvement initiatives

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