Clinical Trials Data Coordinator - Impactful Role

The Sarah Cannon Research Institute in Denver, Colorado seeks a detail-oriented professional to support clinical trial processes. You will assist with document generation, reporting, and ensuring compliance with regulations. A Bachelor's degree and knowledge of GCP are preferred, along with healthcare or clinical trials experience.This role directly impacts the advancement of cancer treatments, contributing to crucial research that transforms patient care. Join us to make a difference and enhance the fight against cancer.J-18808-Ljbffr