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Associate Director, Clinical Science
Natera Remote Posted 4 days ago
About the role
Join Natera as the Associate Director, Clinical Scientist in Oncology.
What you'll do
- 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
What you'll need
Natera lists the full requirements on its posting.