A global clinical research organization is seeking a Clinical Research Associate (CRA) to monitor clinical sites and ensure compliance with study protocols. This role requires at least 1 year of on-site monitoring experience, preferably in oncology solid tumors. Responsibilities include conducting site visits, managing regulatory submissions, and collaborating with site staff for recruitment. The position offers competitive compensation based on experience, with a potential base pay range of $71,900.00 - $169,300.00.