Minimum of 2 years of experience as a Clinical Research Coordinator in oncology.
Demonstrated ability to screen, recruit, and consent patients for clinical trials.
Proficiency in conducting study visits, including obtaining vital signs, performing phlebotomy, and conducting ECGs.
Experience with chart review to assess patient eligibility for oncology clinical trials.
Strong understanding of clinical research processes and oncology trial workflows.
Ability to travel between multiple clinical sites to support patient visits and study activities.
Effective communication skills to interact with patients and multidisciplinary research teams.
Strong organizational skills to manage schedules, patient visits, and study documentation.
Experience with data entry and query resolution in various electronic data capture (EDC) systems.
Prior experience working with contract research organizations (CROs) and study sponsors.
Familiarity with regulatory requirements and documentation processes in clinical research.
Ability to work collaboratively within a multi-disciplinary research team.
Attention to detail and commitment to maintaining high standards of data quality and patient care.
Travel: Local travel required to Glendale, Long Beach, Fountain Valley, and Whittier clinics
