Study Lead Statistician - Remote

Overview

The primary role of this position is to provide statistical support for multiple clinical studies across all phases of clinical development. Apply statistical principles and techniques to a wide range of problems within the clinical development environment with the supervision of more senior staff.

In Short

• 5+ years of clinical trials experience.
• Hands on SAS experience is required.
• Regulatory interaction payer experience.
• Perform all duties and responsibilities associated with the Study Lead Statistician role.
• Attend Clinical Study Team meetings and provide all required statistical input related to strategy and operations of the clinical study.
• Plan and execute statistical contributions to Study Outlines, protocols, Statistical Analysis Plans (SAPs), and other key-study related documentation.
• Stay abreast of latest developments in the field of statistics in drug development.
• Must be solution-oriented and willing to educate study team members in appropriate interpretation of designs and results.

Requirements

• PhD in statistics or related field and at least 6 years of industry experience or MS in statistics or related field and at least 10 years of industry experience.
• Comprehensive knowledge of clinical trials methodology, regulatory requirements, and proficient SAS programming skills.
• Proficient in Microsoft Office.
• Excellent written and verbal communication skills.
• Experience with people management and development of staff.
• Excellent interpersonal and project management skills.
• Able to collaborate effectively with internal and external study management teams.

Benefits

• This posting is for Contingent Worker, not an FTE.