Looking for a strong Clinical Research Coordinator with 3+ years of experience for a Study Coordinator contract position.

Where: ONSITE in San Diego, California - NO option for remote flexibility

Duration: 4-6 month contract, possibility of extension

Therapeutic Area: Ophthalmology - experience with this indication is not required

Responsibilities:

• Chart review
• Data entry and data migration
• Assist with study visits
• Sample collection and processing - excluding venipuncture and study drug administration
• Pre-screening for eligibility to protocol
• Query resolution
• Audit preparation – monitoring visits
• AE monitoring
• Consenting
• Scheduling and appointment reminders
• Source document creation
• Administrative tasks – maintaining study binder, regulatory filing, etc.
• Regulatory document maintenance, preparation, and submission of study level IRB/Regulatory documents from approved templates