Sr CRA (Level I) - FSP

The Sr CRA is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies, ensuring compliance with AZ Procedural Documents and international guidelines. They actively participate in Local Study Team meetings, manage study supplies, and perform monitoring visits both remote and onsite. Additionally, they ensure timely resolution of study-related issues and maintain inspection readiness at all times.

A minimum of 3-5 years' experience as a monitor in clinical research, with special expertise in oncology. A valid driving license is required, and the ability to travel internationally as needed. Experience with ICH-GCP and local regulations is essential.