Job Overview
- Coordinate Clinical Studies adhering to the principles of Good Clinical Practice
- Collect initial medical background from patients and other appropriate sources
- Work as a cohesive team member coordinating assigned studies and backing up other studies
- Educate and provide information to patients and families regarding clinical trials
- Assist and support recruitment with prescreen activities and other activities related to subject recruitment
- Attend study related training and site initiation meetings
- Inventory, handle, and maintain accountability for study supplies and investigational product
- Facilitate study monitoring visits and prompt resolution of all study related queries
- Maintain professional and appropriate interactions with sponsors and all other study related personnel, subjects, families, and staff members.
- Other duties as assigned
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