ONSITE: Houston, TX
CONTRACT: 9 month contract, possible extension
REQUIRED: Clinical Research experience
Clinical Research Coordinator
Job Description
Responsibilities/ Job Duties:
- IPs
- Appointment Reminders
- Scheduling
- Chart Review
- Pre-screening for eligibility to protocol
- Data entry and data migration
- AE Monitoring
- Assist with Study Visits, sample collection and processing - excluding venipuncture and study drug administrationMedical Record Retrieval
- Study visit and audit preparation – monitoring visits
- Consenting
- Administrative tasks – maintaining study binder, regulatory filing, etc
- Query Resolution
- Source Document Creation
- Regulatory document maintenance, preparation, and submission of study level IRB/Regulatory documents from approved templates
Minimum Education and Experience Qualification Requirements:
2+ years of experience as a Clinical Research Coordinator
Ophthamalogy experience preferred
Schedule/ Shift:
Monday through Friday business hours