Biostatistician

Overview

Medpace is expanding its Biostatistics team in Central London or Stirling. In this role you will lead biostatistical activities for clinical trial projects, ensuring delivery within timeframes and quality, and representing the Biostatistics function at conferences and external meetings. You will contribute to protocol development, design data analysis plans, and program analyses, while communicating results to medical writing. This is a growth opportunity toshape drug development in a global CRO.

Pay / Benefits

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Responsibilities

• Contribute to clinical development plan preparation and review study protocols with statistical methodologies
• Develop detailed Data Analysis Plans for assigned projects
• Program study analyses, review results, and prepare statistical methods sections for reports
• Define CRF and database design and data cleanup requirements for analysable variables
• Communicate statistical results to medical writing to ensure proper interpretation

Key requirements

• Ph.D. in Biostatistics / Statistics / Medical Statistics
• Experience in SAS Programming
• Knowledge of advanced statistical methods and the pharmaceutical industry
• Knowledge of regulatory requirements/guidelines for drug development
• Previous experience in a pharmaceutical or CRO (preferred)
• Effective communication and presentation
• Collaborative teamwork
• Cross-functional engagement
• SAS programming
• Development of Data Analysis Plans
• Statistical methodologies knowledge

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