POSITION SUMMARY:

Join Natera as the Associate Director, Clinical Scientist in Oncology. You will execute clinical development strategies for our early cancer detection and cell-free DNA (cfDNA) In Vitro Diagnostic (IVD) portfolio, driving the design and execution of rigorous clinical studies that directly impact patient care. Every sample represents a real person, and you will take ownership of study activities, clinical strategy, and the timely delivery of high-quality data.

PRIMARY RESPONSIBILITIES:

Develop rigorous study concepts, including study design, schedule of assessments, objectives/endpoints, and eligibility criteria
Integrate stakeholder feedback and direct protocol authoring; use data to respond to health authority feedback
Support regulatory interactions and author clinical sections for regulatory correspondence and submissions, including briefing documents, presentations, and Investigational Device Exemption (IDE), IND, and NDA filings
Provide protocol training and contribute directly to Case Report Form (CRF) design
Ensure study manuals align with the protocol and engage investigators directly in study design methodology to ensure alignment with research objectives
Actively participate in pre-site selection discussions, site initiation visits, and investigator meetings to drive successful study execution
Contribute to and oversee real-time clinical data reviews, including the rigorous oversight of Contract Research Organizations (CROs) when applicable
Participate in the review and management of safety reports and submissions, treating quality as foundational
Support project teams with the conduct of clinical studies, including trials registration, results reporting, and the monitoring of emerging clinical and safety data trends
Consult on data management deliverables, clinical monitoring activities, interim analyses planning, and Data Safety Monitoring Board or Steering Committee meetings
Serve as a clinical science representative in internal and external meetings, pushing for clarity and action
Deliver unvarnished, data-backed updates on clinical timelines to senior management, pushing for clarity and outcome-driven decisions to meet program milestones
Support advisory boards and deliver direct, scientific presentations.
Drive clinical research plans, spanning company and investigator-initiated studies
Think team by partnering directly with senior leaders across functions to optimize clinical development and drive strategic execution without needing translation layers
Build data-driven, strategic relationships with Key Opinion Leaders (KOLs), consortiums, and clinical sites
Develop Standard Operating Procedures (SOPs) and analyze complex data.
Ensure strict compliance with HIPAA/PHI regulations and maintain all training requirements
Adapt to evolving clinical needs, taking ownership of tasks that move the work forward without waiting for a finished playbook

QUALIFICATIONS:

Ph.D., RN, MS, or B.S. in a scientific field; advanced degree preferred (MS, PharmD, MD, or PhD)
8–10+ years of clinical research experience, including 3–5+ years in a management role
Experience in oncology and early cancer detection is highly preferred
Experience with project management, clinical research execution, and rigorous scientific writing
Experience with In Vitro Diagnostics (IVD) is a plus
Deep knowledge of regulatory standards and Good Clinical Practices (GCP) is required

KNOWLEDGE, SKILLS, AND ABILITIES:

Think analytically, testing assumptions with data to troubleshoot and solve complex problems
Clear, direct oral and written communication skills with rigorous attention to detail
Think team by pulling cross-functional partners into the work, operating seamlessly across boundaries to advance clinical objectives
Proficiency with Google Workspace and Microsoft Office suites
Operate with pace and precision as the science, product surface, and business continue to evolve
Execution-focused leadership and a rigorous work ethic
Apply business knowledge, exercise data-driven judgment, and escalate issues without hesitation
Rigorous project management, organizational, and interpersonal skills.
Apply an ownership mindset, using data to push for action, close gaps, and deliver clinical outcomes
Demonstrate strategic and flexible thinking to untangle ambiguous problems and deliver actionable solutions

The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years & depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.

Remote USA

$172,100—$215,150 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.

The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.

WHAT WE OFFER

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!

For more information, visit www.natera.com.

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.

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.

Link: https://www.natera.com/notice-of-data-collection-california-residents/

Please be advised that Natera will reach out to candidates with a @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.

For more information:
- BBB announcement on job scams
- FBI Cyber Crime resource page

Remote USA 172100 - 215150 USD

Natera

Associate Director - Clinical Science

About the Job

Requirements

Responsibilities

Desired Qualifications

About the Company

Natera

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