Senior Principal Statistician

Remote – US based candidates only, no visa sponsorship available.

About the role

This role will turn data into practical insight that improves visibility, decision-making, and business performance. You will partner with business, technical, and operational stakeholders to build reporting, surface trends, and translate analysis into action. The position offers the opportunity to strengthen data-driven execution and help teams focus on the metrics that matter most within a life sciences environment.

Responsibilities

• Lead statistical design and analysis for Phase I-IV clinical studies and regulatory submissions
• Collaborate with cross-functional teams to optimize study protocols and reporting timelines
• Develop and implement statistical strategies and protocols for clinical trials
• Review data capture systems; validate data for accuracy and reliability
• Write and oversee statistical analysis plans and ensure quality of CRO deliverables
• Act as a statistical subject matter expert for clinical reporting and respond to inquiries from regulatory agencies

Requirements

• MS or MPH in statistics or related field with 4+ years of experience in the pharmaceutical or biotechnology industry or PhD in statistics or related field with 2+ years of experience
• Expertise in clinical trial design and statistical analyses, including complex methods and regulatory guidelines
• Proficiency in SAS and R programming; knowledge of additional languages is advantageous
• Familiarity with ICH Guidelines and CDISC standards in drug development
• Strong attention to detail and ability to work independently in a fast-paced environment

Benefits

• Medical, dental, and vision insurance coverage
• 401k retirement savings plan with company contributions
• Flexible paid vacation policy to support work-life balance
• Discretionary annual cash bonus and equity grants opportunities

Pay

$156,000 – $234,000 annually