Director, Clinical Science

10+ years of pharma/biotech industry experience in clinical development in oncology clinical trials

Deep understanding and preferably experience in oncology molecular diagnostics, oncology companion diagnostics or early cancer detection

Experience in data review, data cleaning, managing and interpreting clinical trials results as well in writing clinical trial protocols

Possesses sound foundational knowledge of FDA and other major country regulations and detailed knowledge of Good Clinical Practice other regulations governing clinical research

Experience with managing direct reports, ensuring that roles are performed in accordance with job descriptions and that training is conducted and maintained appropriately

Familiarity with Google and Microsoft suites

Natera is seeking a highly motivated and experienced Clinical Scientist to support the development and execution of our innovative Oncology programs.

Director, Clinical Science

will ensure the successful execution of clinical development programs and deliverables in partnership across the organization, with external vendors, and with external academicians and collaboration partners.

The Director, Clinical Science will be accountable to jointly develop clinical program strategy and work collaboratively together with other functional representatives to assure that activities are executed within expected scope, compliance, budget, and timelines.

Develop study concepts, including study design, schedule of assessments, objectives/endpoints, and eligibility criteria

Collaborate cross-functionally to develop Protocol and ICF documents / amendments and present these to governance committee and early clinical development team meetings as required