Associate Director of Biostatistics

This is an exciting opportunity to lead a team of statisticians advancing adoption of Natera’s oncology portfolio of cutting‑edge molecular diagnostic tests. As an Associate Director in Biostatistics, you will leverage your deep applied statistics and leadership background to guide the design and interpretation of Natera sponsored clinical studies ensuring scientific rigor and meaningful clinical insights across oncology programs. This position will play a central role in defining the team’s vision, fostering excellence in biostatistics deliverables, and cultivating a high‑performing, collaborative environment that drives long‑term success. Primary Responsibilities Direct a team of biostatisticians, taking responsibility for their individual deliverables and growth (technical and professional) Oversee Biostatistics contributions to oncology product clinical validation projects Lead development of novel statistical approaches and simulations to support innovative study designs. Produce, review, and standardize high‑quality documentation for cross‑functional internal and external collaborators and stakeholders Identify risks, communicate concerns, and champion solutions to cross‑functional project teams Continuously improve the efficiency and efficacy of team through innovative techniques and strategies Qualifications Advanced degree (Ph.D. or M.S.) in Biostatistics, Statistics, or a related quantitative field (Ph.D. preferred) 7+ years of experience in clinical trial biostatistics Strong knowledge of survival analysis, censoring, and other advanced statistical techniques relevant to oncology Expertise with study design innovation and power/simulation approaches Proven track record in mentoring and developing junior staff Ability to communicate complex statistical concepts clearly to both technical and non‑technical audiences and foster collaborative, cross‑functional partnerships Knowledge, Skills, and Abilities Strong technical leadership and strategic thinking. Proven success leading and developing teams. Deep expertise in statistical methods for diagnostics and clinical trials, including FDA requirements. Effective collaborator across diverse technical disciplines. Clear, high‑quality scientific and technical communication. Familiarity with NGS, ctDNA, and molecular oncology preferred. Location: Remote – United States Compensation: $174,400 - $218,000 USD Our Opportunity Natera™ is a global leader in cell‑free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives. What We Offer Competitive benefits: comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents; free testing; fertility care benefits; pregnancy and baby bonding leave; 401k; commuter benefits and more. Generous employee referral program. EEO Statement Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide. Equal Opportunity Statement All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws. If you are based in California, we encourage you to read this important information for California residents. #J-18808-Ljbffr