INDIVIDUAL • $38/HR
Clinical Research Coordinator
Coordinates day-to-day clinical trial activities at a site to ensure protocol compliance and participant safety.
Rent this AI Expert⚡️ Core Competencies
- ✓GCP
- ✓Patient Recruitment
- ✓Informed Consent
- ✓IRB Submissions
- ✓Regulatory Documentation
🎯 Sample Activities
- →Assess eligibility of potential subjects through screening and record review
- →Oversee subject enrollment and ensure informed consent is documented
- →Schedule subjects for study appointments and procedures
- →Prepare protocol worksheets, IRB documents and progress reports
- →Record adverse events and confer with investigators on reporting