Director of Statistical Programming

This is an exciting opportunity to lead Natera’s Statistical Programming team, specifically focused on advancing our oncology portfolio through high-impact, practice-changing clinical trials.

As a Director, you will provide strategic and technical oversight for all statistical programming activities supporting the clinical validation and utility of Natera’s cutting-edge molecular diagnostics tests.

The ideal candidate possesses a proven track record, strong leadership and communication skills, and a deep expertise in clinical trials, programming, and regulatory deliverables.

• PRIMARY RESPONSIBILITIES
• Team Leadership: Build, mentor, and direct a high-performing statistical programming team, fostering technical excellence and overseeing their professional development.
• Functional

Oversight: Provide strategic direction and standards for the programming function, securing alignment with oncology clinical development goals and department infrastructure needs.

• Submission Leadership: Act as the primary programming lead for regulatory submissions (e. g., 510(k), CTA/CDx, and PMA), ensuring all deliverables meet rigorous global standards.
• Analysis & Reporting: Direct the generation and validation of analysis datasets and TLFs, ensuring data integrity and regulatory compliance with ICH, GCP, and FDA 21 CFR Part 11.
• Development, Standards, and

Validation: Lead the development, validation, and review of efficient R code to support statistical analyses and deliverables.

Enforce departmental standards for programming maintenance and code integrity.

Facilitate cross-functional standards (e CRF design, DMPs).

• Infrastructure: Lead the development and maintenance of scalable programming infrastructure for the larger Biostatistics department.
• Interdisciplinary Partnership: Partner with Biostatistics, Clinical Operations, Data Management, and Regulatory to integrate programming expertise into clinical study execution.

QUALIFICATIONS

• Minimum 10 years of relevant industry experience supporting clinical trials in diagnostics, biotechnology, pharmaceuticals, or related industries.

At least 5 years leading a team.

• Advanced degree in Biostatistics, Statistics, Computer Science, or a related field.
• KNOWLEDGE, SKILLS, AND ABILITIES
• Expert working knowledge of R for clinical trial reporting; experience maintaining statistical packages and computing environments under version control.
• In‑depth knowledge of CDISC standards including SDTM and ADa M.
• Proven track record of producing high‑quality analysis output for regulatory audiences (FDA) and internal stakeholders.
• Proven record of hiring, mentoring, and developing a successful, productive team.
• Demonstrated ability and enthusiasm for working on cross‑functional teams with members of diverse technical backgrounds.
• Exceptional problem‑solving skills and attention to detail.
• Prior experience with NGS, genetics, and/or oncology molecular diagnostic testing a plus.

BENEFITS

Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents.

Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits.

Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more.

We also offer a generous employee referral program!

Remote USA

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.

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.

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