Health Care Specialist
About The Position
The Clinical Research Quality Management Administrator reports to, and is directly responsible to, Associate Director for Administration ( ADA ) for all matters pertaining to the systematic oversight, monitoring, and improvement of clinical trials activities. This role ensures that all oncology trials-including investigator-initiated ( IIT ) industry-sponsored, and national cooperative group studies-are conducted in adherence to National Cancer Institute ( NCI ), Designs and maintains monitoring plans to endure all clinical teams are prepared for internal and external inspections Supports and coordinates the Data Safety and Monitoring Committees ( DSMC ), following the FPBCC Data Safety and Monitoring Plan ( DSMP ), Protocol Review and Monitoring Systems ( PRMS )
Requirements
- 7 years
Responsibilities
- systematic oversight
- monitoring
- improvement of clinical trials activities
- ensures that all oncology trials are conducted in adherence to National Cancer Institute ( NCI )
- Designs and maintains monitoring plans to endure all clinical teams are prepared for internal and external inspections
- Supports and coordinates the Data Safety and Monitoring Committees ( DSMC ), following the FPBCC Data Safety and Monitoring Plan ( DSMP ), Protocol Review and Monitoring Systems ( PRMS )
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What This Job Offers
Job Type
Full-time
Education Level
No Education Listed
Number of Employees
11-50 employees
