Senior Manager Biostatistician Consultant - Remote

Overview

This position involves working directly with a single sponsor while benefiting from the security and career opportunities of a global CRO. The Senior Manager Biostatistician Consultant will work with study teams to design protocols, draft statistical analysis plans, and perform statistical analyses for regulatory submissions.

In Short

• Work directly with study teams and project statisticians.
• Contribute to the design of early/late-stage protocols.
• Draft protocols and amendments.
• Develop and write statistical analysis plans.
• Perform statistical analyses for interim and final reports.
• Support submission activities for safety and efficacy.
• Attend and contribute to study team meetings.
• Collaborate with Statistical Programmers and Data Managers.
• Leadership skills are essential for organizing study deliverables.
• Client-facing role requiring independent work.

Requirements

• MS or PhD in Statistics or Biostatistics.
• PhD +4 years or MS +9 years of clinical trial experience.
• Hands-on experience in Phase I/II/III clinical trials.
• Proficiency in SAS programming; R programming is desirable.
• Excellent oral and written communication skills.
• Experience with regulatory submissions is a plus.

Benefits

• Opportunity to work for a global CRO.
• Supportive company culture.
• Professional development opportunities.
• Work in a high-trust environment.
• Engagement in innovative drug development.