Principal Biostatistician

Precision Medicine Group is seeking a Principal Biostatistician to provide statistical support for all phases of clinical development. The Principal Biostatistician will be responsible for writing and reviewing statistical sections of protocols and statistical analysis plans, conducting statistical analyses, presenting results, and developing SAS programs.

Responsibilities include:

• Generating and verifying randomization schedules.
• Developing and reviewing statistical methods of the clinical study protocol.
• Providing and verifying sample size calculations.
• Authoring statistical analysis plans.
• Generating analysis datasets, tables, figures, and listings using SAS.
• Performing quality control for statistical based SAS programs.
• Providing statistical analysis and reports to Data Monitoring Committees (DMCs).
• Reviewing statistical sections of clinical study reports.
• Leading all statistical activities for studies within timelines.

Requirements:

• Master's degree or equivalent in Statistics, Biostatistics, or related field with 10+ years experience; PhD degree in Statistics, Biostatistics, or related field with 7+ years experience.
• Experience with SAS.
• Knowledge of industry standards such as the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA guidelines.
• Broad knowledge and superior understanding of advanced statistical concepts and techniques.

The role offers:

• Opportunity to work remotely.
• Chance to lead statistical activities for studies.
• Involvement in the development and maintenance of departmental procedures and standards.