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