What are the responsibilities and job description for the Clinical Research Regulatory Coordinator position at Marshall Health Network?
Cabell Huntington Hospital is seeking a full-time Clinical Research Regulatory Coordinator.
This position is responsible for the collection of data for the purpose of creating ad hoc reports in addition to clerical duties related to clinical trials.
Specific Responsibilities :
- Knowledge of FDA regulatory requirements, commonly-used concepts, practices and procedures.
- Possesses extensive computer experience and the ability to learn job specific computer programs.
- Facilitates timely safety reporting to the IRB.
- Prepares proposed clinical trials for IRB review and approval.
- Monitors the administration and progress of clinical trials
Education :
Experience :
The kind of position-related experience includes :
Familiarity with reading patient charts / records an asset.
Basic computer knowledge.
Microsoft Office
Knowledge of medical terminology desired.
Typing speed of 40 wpm
Organization and time management skills
