Senior Biostatistician Consultant

Job Summary

Senior Biostatistician Consultant is a remote, 24-month contract position responsible for collaborating with study teams to design protocols, draft statistical analysis plans, and perform statistical analyses for regulatory submissions.

Key Responsibilities

• Contribute to the design of early/late-stage protocols and draft statistical analysis plans
• Perform statistical analyses for interim and final reports submitted to regulatory agencies
• Support submission activities and collaborate with Statistical Programmers and Data Managers on study deliverables

Required Qualifications

• MS or PhD in Statistics or Biostatistics
• PhD +4 years or MS +9 years of clinical trial experience in biotechnology or pharmaceutical companies
• Hands-on experience with Phase I/II/III clinical trials and proficiency in SAS programming; R programming is desirable
• Previous experience with regulatory submissions is desirable