3 * Clinical Research Associates

Discover International; United States; On-site; USD 85,000 - 120,000; Full time

Job summary

Discover International is expanding its Clinical Research team, seeking experienced CRAs with ophthalmology trial background and sponsor-side exposure. The role involves monitoring ophthalmology sites across regions, ensuring protocol and ICH-GCP compliance, and collaborating with investigators. Travel as required.

Ideal candidates will have CRA/LCRA experience, strong communication skills, and the ability to manage site performance from start-up to close-out.

Qualifications

• Ophthalmology clinical trial experience required.
• Sponsor-side experience is a must.
• Strong knowledge of ICH-GCP and trial processes.
• Willingness to travel and monitor sites.
• Previous CRA/LCRA experience preferred.

Responsibilities

• Conduct monitoring visits and oversee assigned clinical trial sites.
• Ensure compliance with protocols, ICH-GCP, and applicable regulations.
• Partner closely with investigators and site teams.
• Monitor recruitment, data quality, and study performance.
• Identify and resolve site issues while maintaining high-quality trial execution.

Skills

Ophthalmology trials

Sponsor experience

ICH-GCP knowledge

Site monitoring

Communication skills

Travel willingness

Job description

Our client is expanding his Clinical Research team and looking for experienced Clinical Research Associates (CRAs) with ophthalmology clinical trial experience and sponsor-side experience.

• LCRA – Western Region | Ophthalmology
• CRA – Southwest | Ophthalmology
• CRA – Midwest | Ophthalmology
• Previous CRA/LCRA experience
• Ophthalmology clinical trial experience
• Sponsor experience is a MUST
• Strong knowledge of ICH-GCP and clinical trial processes
• Experience with site monitoring from start-up through close-out
• Excellent communication, organizational, and relationship-building skills
• Willingness to travel as required
• Conduct monitoring visits and oversee assigned clinical trial sites
• Ensure compliance with protocols, ICH-GCP, and applicable regulations
• Partner closely with investigators and site teams
• Monitor recruitment, data quality, and study performance
• Identify and resolve site issues while maintaining high-quality trial execution