Paula Pheley
Clinical Research Coordinator
- Reviews agency rules for proposal submission
- Formats proposals to meet agency rules
- Prepares data collection forms
- Prepares IRB applications
- Prepares drafts of informed consent forms
- Prepares grant budgets
- Background work for budget e.g., contacting companies in search of appropriate equipment
- Assists with literature review and gathering of articles
- Prepares grant documents for ORSP approval
- Tracks post submission requirements