Ophthalmology Clinical Research Associate

Responsibilities

• Support the planning, execution, and monitoring of ophthalmology clinical trials across multiple study sites.
• Serve as a key point of contact for study teams, sites, and sponsors to ensure smooth communication.
• Ensure trial activities adhere to ICH-GCP guidelines, FDA regulations, and study protocols.
• Track study timelines, patient enrollment, and data quality while identifying and addressing risks.
• Affiliate with site initiation, monitoring visits, and closeout activities.

Requirements

• 2+ years of clinical research experience with exposure to site or sponsor-side trial support.
• Ability to travel to sites 8-10 days on site per month.
• 2+ years of onsite monitoring experience.
• Experience with ophthalmology or ophthalmic studies.
• Working knowledge of GCP, FDA regulations, and clinical trial processes.

Pay

$90,000 - $140,000 base salary, Depending on Experience and Level

Benefits

• Full Comprehensive Benefits: Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law.

Keywords

• ophthalmology
• clinical research associate
• CRA
• clinical trials
• GCP
• FDA regulations
• site monitoring
• clinical operations
• ophthalmic studies
• CTMS
• EDC
• regulatory compliance
• patient enrollment
• study coordination