Senior Biostatistician

This is a fully remote position, open to applicants in Taiwan.

📋 Description

• Create statistical analysis plans and reporting specifications for clinical studies ranging from simple to moderate complexity.

• Identify and articulate suitable statistical methods for analyzing clinical data.

• Collaborate with statisticians regarding methodology, study design, therapeutic areas, and data interpretation.

• Design templates and specifications for output presentations.

• Conduct statistical analyses and provide interpretations of the results.

• Develop or perform quality control on analysis programs that implement statistical analysis plans.

• Approve final databases for freezing or locking.

• Evaluate model assumptions relevant to statistical analyses.

• Coordinate data summarization and analysis efforts with programmers, writers, and clinicians.

• Generate statistical reports and statistical sections for clinical study reports.

• Offer statistical expertise to project teams.

• Act as the primary functional representative within project teams.

• Assist in the preparation and review of clinical study protocols.

• Create dummy and final randomization plans.

• Engage in the development and review of CRF, data edit specifications, and critical variable lists.

• Estimate resource needs and project timelines in collaboration with project and functional managers.

• Meet with clients to address statistical matters.

• Keep abreast of and share knowledge regarding company and industry protocols and methodologies.

• Execute billable tasks in accordance with WuXi CDS policies, procedures, and standard operating procedures.

⛳️ Requirements

• MS degree with 3 years of experience or a PhD degree in statistics or biostatistics with 2 years of experience.

• Proven expertise across various statistical domains.

• Proficient in planning, implementing, and overseeing statistical processes for clinical studies.

• Exceptional written and verbal communication skills.

• Proficient in reading, writing, and speaking English.

• Strong understanding of the drug development process.

• Comprehensive knowledge of SAS procedures and sound programming practices.

• Familiarity with FDA and EMEA guidelines and requirements for the reporting of clinical trial data.

• Commitment to ongoing statistical training and development of new methods and techniques.

🏝️ Benefits

• Engage in purpose-driven work that contributes to clinical trials in renal, cardiometabolic, and oncology therapies.

• Flexible hybrid or remote working options, based on location and role.

• Opportunities for career advancement and professional development.

• Access to a global network of scientific leaders.

• Employee wellness programs that support work-life balance, health, and team connections.

• Participation in global engagement surveys.

• Recognition programs to celebrate achievements.

• Team-building activities to foster collaboration.

• Global opportunities with exposure to a variety of projects and clients.

• Competitive salary and benefits package tailored to your skills and experience.