Senior Biostatistician

🔥 20 hours ago

🇹🇼 Taiwan – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 11%

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.

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Emerald Clinical

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 2000

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Emerald Clinical is a leading global clinical research organization (CRO) founded in the Asia‑Pacific region that provides end‑to‑end clinical trial services to biopharmaceutical, medical device, and diagnostic companies. With about 25 years of experience and a team of 800+ operating across 40+ locations worldwide, Emerald Clinical manages trials across all phases including registration and post‑marketing studies, and offers clinical operations, project management, and trial staffing support. The company emphasizes scientific expertise, operational excellence, and global reach to support drug and device development.

📋 Description

• Develop statistical analysis plans and reporting specifications for simple to moderate clinical studies • Develop and describe appropriate statistical techniques for clinical data analysis • Collaborate with statisticians on methodology, study design, therapeutic areas, and data analysis • Design shells and specifications for outputs • Perform statistical analyses and interpret results • Develop or QC analysis programs implementing statistical analysis plans • Approve final databases for freeze/lock • Assess model assumptions for statistical analyses • Coordinate data summarization and analysis with programmers, writers, and clinicians • Develop statistical reports and statistical sections of clinical study reports • Provide statistical expertise to project teams • Serve as primary functional representative on project teams • Contribute to clinical study protocol preparation and review • Create dummy and final randomization schemes • Participate in CRF, data edit specification, and critical variable list development and review • Determine resource projections and project schedules with project and functional managers • Visit clients to discuss statistical issues • Maintain and share knowledge of company and industry procedures and methodologies • Perform billable work according to WuXi CDS policies, procedures, and SOPs

🎯 Requirements

• MS degree with 3 years of experience OR PhD degree in statistics or biostatistics with 2 years of experience • Demonstrated expertise in multiple statistical areas • Demonstrated ability to plan, implement, and monitor statistical processes for clinical studies • Excellent written and oral communication skills • Read, write and speak English • Solid knowledge of the drug development process • Solid knowledge of SAS procedures and good programming practices • Knowledge of FDA and EMEA guidelines and requirements for reporting clinical trial data • Continued statistical training on new methods and techniques

🏖️ Benefits

• Purpose-driven work contributing to clinical trials in renal, cardiometabolic, and oncology therapies • Hybrid or remote working arrangements, depending on location and role • Career growth and learning opportunities • Access to a global network of scientific leaders • Employee wellbeing programs promoting work-life balance, health, and team connection • Global engagement surveys • Recognition programs • Team-building events • Global opportunities and exposure to diverse projects and clients • Competitive salary and benefits package tailored to skills and experience