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Senior Biostatistician

đź•’ July 22

🇬🇧 United Kingdom – Remote

⏰ Full Time

đźź  Senior

đź§Ş Clinical Research

🇬🇧 UK Skilled Worker Visa Sponsor

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đź‘» Ghost score 54%

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Logo of Parexel

Parexel

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.

đź“‹ Description

• Lead research design and analytical strategies • Provide input into protocols • Develop and review statistical analysis plans • Author/co-author reports, abstracts, and manuscripts • Advise, provide guidance, and oversee quality control of statistical deliverables • Act as functional lead within study teams and direct Biostatistical activities • Perform intricate statistical analyses and provide input to statistical reports • Provide input to analysis plans, statistical reports, and statistical sections of integrated clinical reports • Advise on analyses from the proposal process through the project life cycle • Coach and mentor junior department members • Liaise with biostatistical and company departments to optimize global efficiency • Coordinate Biostatistics project activities within timelines and budget • Coordinate with clients regarding data analysis, scope of work, and budget • Represent Parexel at client meetings

🎯 Requirements

• Masters Degree in Statistics (or equivalent) plus a minimum of 6 years industry (or directly relevant) experience OR Ph.D. in Statistics (or equivalent) plus 4 years 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 (desired) • Masters or Ph.D. level education in biostatistics, statistics, mathematics, or another relevant discipline • 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 • Ability to develop complex analysis strategies and execute them using efficient programming techniques • Ability to review analysis data sets and quality control statistical analysis deliverables

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