Clinical Research Coordinator II - Medicine Clinical Trials Office
About The Position
A Clinical Research Coordinator (CRC) II position is currently available within the Medicine Clinical Trials Office. Responsibilities will include activities such as data collection and management of patient clinical information, timely collection of protocol related samples including shipment to outside entities as required, obtain informed consent, collect, maintain and organize study information, and assist with other day-to-day operations as required. Under minimal supervision, the Clinical Research Coordinator II will manage a workload that includes studies of increased complexity.
Requirements
- Minimal supervision required
- Ability to manage studies of increased complexity
Responsibilities
- Coordinates the clinical assessments of the study subjects
- Analyzes and assists in interpreting moderately complex clinical research data
- Prepares grant applications and documents
- Assists in protocol submissions (for e.g., Institutional Review Board, Grants and Contracts Office)
- Data collection and management of patient clinical information
- Timely collection of protocol related samples including shipment to outside entities as required
- Obtain informed consent
- Collect, maintain and organize study information
- Assist with other day-to-day operations as required
- Manage a workload that includes studies of increased complexity
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
