Biostatistician II

🕒 July 22

🇬🇧 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.

👻 Ghost score 55%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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

• Independently lead development and execution of statistical aspects for low- to moderate-complexity studies • Develop complex analysis strategies and execute them using SAS or R • Perform intricate statistical analyses and provide input to statistical reports • Collaborate on global, cross-functional teams • 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 • Review analysis data sets and quality-control statistical analysis deliverables • Liaise with biostatistical and other company departments to optimize global efficiency • Coordinate Biostatistics project activities within timelines and budget • Coordinate with clients on data analysis, scope of work, and budget • Translate scientific questions into statistical terms and statistical concepts into layman terms

🎯 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 • 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) • 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