Job Description
Emerald Clinical is seeking a Clinical Research Associate 2 (CRA2) to join the Clinical Operations group. You will oversee site management, monitoring tasks, and regulatory support across trials, ensuring SOP and ICH-GCP compliance. Responsibilities include site identification, feasibility, initiation visits, TMF filing, budget negotiation, and tracking site payments. The role requires 2–5 years on-site monitoring, oncology exposure, and travel willingness. #J-18808-Ljbffr
