Clinical Trials Coordinator

Responsibilities

Under the direction of the Chief Administrative Officer and the Clinical Trials Manager, the Study Coordinator is responsible for the coordination
of complex, high-volume 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 FDA; 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.

**May be hired at a
Public Admin Analyst level, based upon experience and qualifications.**  

Qualifications

• Minimum of three years experience working in FDA governed trials highly desired
• Minimum of three years experience working with complex oncology trials strongly preferred
• Bachelor’s degree preferred

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.

To apply for this position, please copy and paste the following link into your browser address bar:
https://ucla.contacthr.com/74066205