Clinical Research Assistant I - Early Cancer Detection
City of Hope
Duarte, CA
See who City of Hope has hired for this role
Join the forefront of groundbreaking research at the Beckman Research Institute of 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.
Exciting opportunity for a detail-oriented individual! Join us as a Clinical Research Assistant I in which you will manage an assigned set of multiple research protocols to assure efficiency and regulatory compliance of the protocol. Showcase your independent judgment and elevate your career in a role that makes a meaningful impact on groundbreaking research!
As a successful candidate, you will:
To learn more about our Comprehensive Benefits, please CLICK HERE.
Exciting opportunity for a detail-oriented individual! Join us as a Clinical Research Assistant I in which you will manage an assigned set of multiple research protocols to assure efficiency and regulatory compliance of the protocol. Showcase your independent judgment and elevate your career in a role that makes a meaningful impact on groundbreaking research!
As a successful candidate, you will:
- Play an active role in the recruitment of participants to identify their eligibility for clinical trials.
- Ensure participants are appropriately registered; maintains documentation of participant registration.
- Conduct protocol management for an assigned set of multiple research protocols.
- Maintain current and accurate protocol documentation; notifies investigators of pertinent protocol changes.
- Assist in training and mentoring new clinical research staff members.
- Perform protocol specific clinical duties as required per the research study.
- 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.
- Associate’s Degree.
- Experience may substitute for minimum education requirements.
- Read, identify, and extract pertinent data from medical records.
- Ability to read, write and comprehend medical terminology.
- Bachelor’s degree.
- Familiarity with Electronic Medical Records (EMR) such as EPIC; Clinical Trials Management Systems (CTMS) such as OnCore, LabVantage and RedCap.
To learn more about our Comprehensive Benefits, please CLICK HERE.
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Seniority level
Not Applicable -
Employment type
Part-time -
Job function
Research, Analyst, and Information Technology -
Industries
Non-profit Organizations, Research Services, and Hospitals and Health Care
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