Clinical Trials Data Coord
City of Hope · Duarte, CA · 2 days ago
AnalystFull-time
Responsibilities
- Data abstraction
- CRF completion
- Query resolution
- Sponsor monitor visit coordination
- Maintaining audit-ready data
- Oversight of electronic research records and patient information in the CTMS
Qualifications
- Bachelor’s Degree, relevant experience may substitute for degree
- At least two years of experience related to the conduct of oncology clinical trials
- Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements
Skills
- In-depth knowledge of Good Clinical Practices (GCP)
- Food and Drug Administration (FDA) regulations
- NIH guidelines
- HIPPA regulations
- Clear and timely written and verbal communication skills
- Effective collaboration as a member of the clinical research team
- Communication of protocol deviations or issues related to study execution
- Comprehension, communication, and oversight of study protocols
Benefits
- Pay is based on work experience, qualifications, and work location
Pay
City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.
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