UCLA Health Los Angeles, CA, USA
Responsibilities Under the direction of the CT Administrator, Faculty, Director, and Executive CAO, you will be responsible for assisting in coordination of research activities for pharmaceutical/industry-sponsored, investigator-initiated, and NIH-sponsored clinical trials for the UCLA Institute of Urologic Oncology. Your key responsibilities include: resource planning, troubleshooting and coordinating efficient workflow and turnaround of pre-study tasks with other pre-award staff, and assisting with development of case report forms. This position requires a basic understanding of clinical trials coordination. Proficient computer skills are essential. Contract, may become career Qualifications Demonstrated clinical research experience, with basic knowledge of clinical urology, including working knowledge of good clinical practices for clinical research. Ability to work in more than one environment, travels to participating hospitals, and attend off site staff...