Job Title

Elevate your career as a Clinical Research Associate with a focus on oncology studies. This role includes overseeing site management and compliance while ensuring outstanding study outcomes in a remote or on-site setting. In this senior CRA position, you will engage closely with investigators and study teams. Your responsibilities will include site selection, training site staff, and maintaining compliance with ICH-GCP guidelines. Contribute to the success of critical oncology and cell therapy trials by ensuring that all study processes run smoothly and efficiently. Key Responsibilities: Select and qualify investigators for trials Train and support site staff in study-related tasks Monitor study sites for compliance with guidelines Conduct remote and on-site visit monitoring Ensure accurate documentation and reporting Requirements: Strong background in oncology clinical trials Bachelor's degree in a relevant field Knowledge of ICH-GCP and local regulations Strong communication and collaboration skills Ability to manage multiple priorities effectively Leverage your oncology expertise and transform clinical trial management, enhancing outcomes across critical studies. #J-18808-Ljbffr