Clinical Research Data Coordinator
City of Hope
full-time
Posted on:
Location Type: Remote
Location: California • United States
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About the role
- Responsible for the collection, coordination, processing and quality control of clinical trial data
- Implement and conduct data management and compliance of multiple research projects
- Review, synthesize and abstract information from medical records to extract trial data
- Complete study visits and/or element completion in CTMS to correspond to EDC data entry
- Perform quality assurance checks to ensure the accuracy of data entered
Requirements
- Minimum of an associate degree in life sciences or information systems
- 2-3 years clinical/oncology experience preferred
Benefits
- Health insurance
- Retirement plans
- Paid time off
Applicant Tracking System Keywords
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Hard Skills & Tools
data managementquality controldata processingdata entryquality assuranceclinical trial data collectionmedical record synthesisdata abstractioncompliance managementresearch project coordination