# Associate Director, Clinical Science at Natera

Natera is hiring an Associate Director, Clinical Science for a remote role open to applicants in United States. Level rates it Little AI ●○○○; you can [apply on Natera](https://jobsbylevel.com/go/2bff864c-c325-43dc-8363-73ed92baf773?utm_medium=ai-agent).

AI Level 1, AI centrality 0 out of 100. Remote (US Remote).

## Details

- Company: [Natera](https://jobsbylevel.com/companies/natera)
- AI level: AI Level 1 (score 0 out of 100)
- Location: Remote (US Remote)
- Posted: November 3, 2026
- Apply: https://jobsbylevel.com/go/2bff864c-c325-43dc-8363-73ed92baf773?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=associate-director-clinical-science-at-natera-ab2bfa

## Prepare for this job

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## Description

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

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