Clinical Research Associate I - Hematology Programs
About The Position
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 in which you will manage an assigned set of multiple research protocols to assure efficiency and regulatory compliance of the protocol, attending clinic as needed, with mentorship by experienced staff.
Requirements
- Associate’s Degree.
- Experience may substitute for minimum education requirements.
- One-year experience working in a health care setting, preferably in research.
Nice To Haves
- Bachelor’s Degree.
- Medical Record, Health Information Systems, clinical trials exposure or related health field.
Responsibilities
- 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.
- Work with supervisor to ensure performance of appropriate levels of quality.
- Process specimens that need to be shipped for analysis.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
