Clinical Research Associate II

Assists in the planning, designing, and executing of clinical studies to assess safety and effectiveness of products. This position works with confidential subjects and company data, and interfaces with a variety of internal and external stakeholders. Responsibilities include drafting informed consent templates, assisting with project timelines, preparing meeting materials, and developing study-related documents. You'll drive study start up, amendment and closeout activities across multiple studies. Motivate clinical sites to meet study endpoints. Collaborate with the Clinical Field team to identify improvements in site activation. Additional responsibilities include tracking regulatory documentation, assisting with Clinical infrastructure maintenance, and providing updates to management.