Associate Director Biostatistician Consultant (24 months contract) at ClinChoice

📋 Description

• Independently contribute to design of early/late-stage protocols across multiple therapeutic areas.
• Draft protocols or amendments and develop/write statistical analysis plans.
• Perform statistical analyses for interim and final regulatory reports.
• Support submission activities and integrated safety/efficacy summaries.
• Represent Biostatistics in client/project team discussions.

🎯 Requirements

• MS or PhD in Statistics or Biostatistics.
• PhD + 6 years or MS + 11 years clinical trial experience.
• Hands-on Phase I–III clinical trial experience; SAS; R desirable.
• Excellent oral and written communication skills.
• Regulatory submissions experience in US/Europe/Japan desirable.

🎁 Benefits

• Equal opportunity employer; values diversity.
• Inclusive, barrier-free recruitment; accommodations on request.
• Client-facing, collaborative culture with strong development.