Clinical Trials Coordinator

Responsibilities

Under the direction of the Department Vice Chair
and the Clinical Trials Manager, the Study
Coordinator is responsible for the coordination of clinical
tasks and conduct of administrative tasks required to successfully conduct
clinical trials within the Department of Radiation Oncology. Responsibilities include preparing and
updating study orders based on an in-depth analysis of the protocol; planning
and coordinating logistics and scheduling study visits with nursing and other
clinical staff within the Department and extra-departmentally; identifying
potential study subjects for recruitment; regular communication with and reporting
to investigators, sponsors, monitors and subjecgts; reporting/recording serious adverse
events and deviations to compliance committees; providing
administrative, regulatory and data management support as needed. Exercise
critical thinking and implement a dynamic, continuous and solution-oriented
approach in the coordination of clinical trials.
Qualifications

Bacherlor's degree strong preferred;

3 years or more experience in FDA governed trials strongly preferred;

3+ years in complex oncology trials strongly preferred.

Self-directed and proactive

Critical thinking skills to be able to implement a dynamic, continuous and solution-oriented
approach in the coordination of clinical trials

Ability to determine the most appropriate and efficient
method of completing each project

UCLA is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected Veteran status.

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