Senior Manager Biostatistician Consultant (remote in UK- Outside IR35) 24 months contract

📋 Description

• Design early/late-stage study protocols across multiple therapeutic areas.
• Draft protocols or amendments and develop statistical analysis plans.
• Perform interim and final statistical analyses for regulatory submissions.
• Support submission activities, including integrated safety and efficacy summaries.
• Attend study team meetings and provide statistical input.
• Collaborate with Statistical Programmers and Data Managers on study deliverables.

🎯 Requirements

• MS or PhD in Statistics or Biostatistics.
• PhD +4 years (or MS +9 years) clinical trial experience in biotech/pharma.
• Hands-on Phase I–III clinical trial experience; proficient in SAS; strong R skills desirable.
• Excellent oral and written communication skills.
• Regulatory submissions experience in US/Europe/Japan/Rest of World desirable.

🎁 Benefits

• Client-facing role with high-trust collaboration.
• Global CRO with a focus on quality and professional development.
• Equal opportunity employer with a diverse workforce.
• Ongoing training and career development opportunities.