Clinical Research Associate II
US Oncology-San Francisco, CA, 94101
SCOPE: Monitors U.S. oncology clinical research phase I-IV trial activities at clinical research study sites to assure adherence to Good Clinical Practices (GCP), International Conference on Harmonisation (ICH), Standard Operating Procedure (SOP), and study protocols. Reviews regulatory documents and prepares site visit reports. Responsible for monitoring up to 30 clinical sites, multiple simultaneous trials, and training sites on research related SOPs. Supports and adheres to the US Oncology Compliance Program, to include the Code of Ethics and Business Standards. ESSENTIAL DUTIES AND RESP...