Experienced Clinical Research Associate for Oncology Trials

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.