Senior Biostatistician

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

📋 Description

• Oversee the resolution of daily operational challenges while enhancing the quality, efficiency, and productivity of statistical and programming functions.

• Manage designated projects by utilizing project management skills alongside statistical and programming methodologies.

• Offer statistical guidance for the design, analysis, and reporting of clinical trials and research initiatives.

• Draft statistical protocol sections, conduct sample size assessments, create randomization specifications, and produce randomization codes.

• Develop Statistical Analysis Plans and respond to feedback from peer statisticians.

• Establish and uphold quality control (QC) and quality assurance (QA) plans for statistical and programming tasks.

• Create and evaluate ADaM dataset specifications and examine SDTM specifications.

• Execute QC validation for analysis datasets, including tables, listings, and figures.

• Lead statistical dry runs and final runs, manage resources effectively, address inquiries, and resolve data-related challenges.

• Review Analysis Data Reviewer’s Guides and integrate comments from data standards reviews.

• Conduct statistical analyses and validations, respond to QC findings, and assist in reporting trial outcomes.

• Contribute to the preparation of Clinical Study Reports and draft statistical reports or relevant sections.

• Perform statistical analyses for abstracts, manuscripts, presentations, and posters.

• Provide statistical insights for CRF design, database and variable structures, data collection, data cleaning, and data validation standards.

• Specify or program database quality acceptance checks and ensure resolution of data quality issues.

• Support data management and trial management teams in the database lock preparation process.

⛳️ Requirements

• A Ph.D. in statistical science, mathematical analysis, or a related field with 2 years of pertinent experience, or a Master’s degree with 4 years of relevant experience.

• Proven ability and consistent performance in relevant roles.

• Completion of all necessary job-related and project-specific training.

• Adhere to applicable Everest and trial sponsor policies, SOPs, and work instructions.

• Ensure proper archiving of study files in line with trial sponsor requirements.

• Plan and execute professional development initiatives.

🏝️ Benefits

• Equal opportunity and accommodations for disabilities available upon request during the recruitment and selection process.

• Opportunities for professional development activities.