Clinical Research Assoc

The Clinical Research Associate helps design and execute clinical research studies, working closely with Natera’s clinical trials, medical education, and scientific communications teams. This role coordinates all aspects of clinical studies, prepares essential documents like consent forms and study protocols and assists with managing study contracts, budgets, and vendor payments. Responsibilities also include tracking clinical trial samples and participant data, monitoring study progress, and providing status updates. Furthermore, they may train CROs, vendors, and investigators, while also providing support and logistical support for clinical studies. The position involves problem-solving, building relationships, and a commitment to expanding personal knowledge and development within the company.