Clinical Research Assistant II - Early Cancer Detection (Hybrid)
Duarte, California
Employer: City of Hope
Industry: Population Sciences
Salary: Competitive
Job type: Full-Time
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 II 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:
Your qualifications should include:
To learn more about our Comprehensive Benefits, please CLICK HERE .
Exciting opportunity for a detail-oriented individual! Join us as a Clinical Research Assistant II 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:
- Manage multiple research protocols, ensuring adherence to protocol requirements and notifying investigators of changes.
- Register patients and maintain accurate documentation throughout the research process.
- Compile and submit data according to protocol guidelines, ensuring compliance with study requirements.
- Actively recruit patients for studies and assist in training new clinical research staff.
- Perform protocol-specific clinical duties and collect specimens for analysis, maintaining confidentiality and safety protocols.
- Collaborate with physicians and nurses to order protocol-related tests and evaluations.
- Identify and communicate protocol and data management issues to supervisors and works on special projects as assigned.
- Maintain professional development through seminars and workshops, ensuring an organized and efficient work environment.
Your qualifications should include:
- Associate's Degree.
- Experience may substitute for minimum education requirements.
- Two years of experience working in a health care setting, preferably in research.
- Bachelor's degree.
- Society of Clinical Research Associates (SOCRA) certification.
- 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 .
Created: 2024-05-12
Reference: 10025933
Country: United States
State: California
City: Duarte
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