Lead Biostatistician for Clinical Trials

Elevate clinical development with Precision Medicine Group as a Lead Biostatistician. Utilize your extensive experience to provide critical statistical oversight and strategic consulting in complex clinical studies.

As a Principal Biostatistician, you will guide clinical trial design and regulatory approaches while writing statistical analysis plans. Your expertise in advanced methodologies such as Bayesian adaptive designs will be essential for ensuring accurate results. Engage proactively with clients and internal teams, mentoring junior statisticians along the way.

Key Responsibilities:

• Consult on clinical trial designs and regulatory strategies

• Develop and review statistical methods for protocols

• Author and verify statistical analysis plans

• Review outputs to ensure accuracy of analyses

• Provide insights to Data Monitoring Committees (DMCs)

Requirements:

• Master’s/PhD in Statistics or Biostatistics

• 10+ years experience (Principal level) or 12+ years (Senior Principal)

• Broad experience with regulatory submissions

• Expertise in SAS and statistical methodologies

• Strong communication and problem-solving skills

Bring your statistical expertise and leadership to support critical clinical programs with Precision Medicine Group.
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