Senior Principal Biostatistician

About the Role

Key Responsibilities:

• Lead all statistical activities for assigned clinical trials.

• Contribute to protocol development aligned with the broader development plan, including drafting statistical analysis plans and managing reporting tasks.

• Support the execution of statistical analyses and offer consultation within cross-functional teams.

• Champion the adoption of innovative methodologies and trial designs under the guidance of the Lead Statistician.

• Partner with clinical, regulatory, and other strategic teams to support data-driven decision-making within assigned programs or indications.

• Collaborate with functions such as data management, programming, and medical writing to ensure timely and high-quality statistical deliverables.

• Participate in external engagements, including work with consultants, advisory boards, regulatory agencies, and presentations at scientific meetings or conferences.

Role Requirements

Basic Qualifications:

• PhD in statistics or a related field with 3+ years of relevant experience, or MS with 7+ years of experience.

• Proficiency in English (spoken and written).

• Strong communication and presentation abilities.

Compensation & Benefits:

• Salary Range (as of 1/1/25 – 12/31/25): $119,700 to $222,300 per year. Final compensation will depend on factors like location, experience, skills, and qualifications.

• Total Rewards: May include sign-on bonuses, stock options, discretionary incentives, 401(k) contributions, and a comprehensive benefits package including health insurance and paid leave (e.g., vacation, sick time, parental leave).

• Employment is on an at-will basis, and compensation may be adjusted based on individual and company performance or market conditions.