Clinical Research Associate I

Join the forefront of groundbreaking research at City of Hope where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research.

Come join us as a Clinical Research Associate I. If you are adaptable, independent, and professional in diverse settings, then this is the right fit for you!

As a successful candidate, you will:

• Conduct protocol management for an assigned set of multiple research protocols.

• Maintain current and accurate protocol documentation; notify investigators of pertinent protocol changes.

• Maintain and complete regulatory documents for IRB, DSMB, and PRMC/CPRMC.

• Compile and submit data on appropriate forms according to protocol requirements.

• Establish and maintain interpersonal relationships with patients, visitors, and other hospital personnel, while assuring confidentiality of patient information.

• Collect and deliver specimens for analysis, using appropriate or specified equipment for collecting and handling specimens; ensure proper labeling and obtain pertinent clinical and protocol information on request forms; develop and maintain knowledge of various aspects of processing specimens, paying particular attention to safety practices.

• Work with physician or nurse to see that protocol related tests and evaluations are ordered per protocol guidelines.

• Play active role in recruitment of patients to study.

• Perform protocol specific duties as required per the research study.