Primarily a training and development role, this position supports and observes clinical site monitoring services both inhouse and in the field whilst developing CRA skills and knowledge. This role has exposure and training in all aspects of the clinical site monitoring services while providing monitoring and site management activities for full-service studies, assessing protocol, SOP, and regulatory compliance.

The Clinical Research Associate helps design and execute clinical research studies. Working closely with Natera’s clinical trials, medical education, and scientific communications teams to accomplish this end. Responsibilities inlcude coordinating all aspects of a clinical study and preparing and developing project and study-related documents. Also track and manage clinical trial samples and participant data.

Oversee multiple oncology trials, ensuring high-quality execution. Provide leadership and mentorship to junior flex team members. Act as Lead SM, training and guiding other Site Managers on study protocols. Develop essential study start-up documents, including SIV agendas. Represent Site Managers and Lead Trial Managers (LTMs) in key meetings.