Ophthalmic CRA II — Global Trials & Impact

Ora; United States; Remote; USD 65,000 - 95,000; Full time

Benefits offered by this job

Healthcare

Flexible PTO

401K plan

Job summary

Ora’s Clinical Research Associate II collaborates with Lead CRA and Line Manager to ensure high-quality study conduct across sites. The role emphasizes ICH/GCP compliance, regulatory documentation, and cross-functional coordination to achieve site readiness and data integrity.

The position requires building strong site relationships, performing monitoring activities, and traveling up to 75% to support study sites globally.

Qualifications

• Bachelor’s degree with 2 years’ experience as a Clinical Research Associate or equivalent.
• Experience with ophthalmic studies is strongly preferred.

Responsibilities

• Develop strong site relationships and maintain continuity through all trial phases.
• Monitor study conduct for ICH/GCP compliance and sponsor SOPs.
• Perform remote and on-site monitoring and oversight activities; ensure data integrity and subject safety.

Skills

Clinical research experience

Ophthalmic experience (preferred)

Attention to detail

Excel

CTMS

EDC

Education

Bachelor’s degree in a life science or related field

Tools

CTMS

EDC

Excel

Job description

Ora’s Clinical Research Associate II collaborates with Lead CRA and Line Manager to ensure high-quality study conduct across sites. The role emphasizes ICH/GCP compliance, regulatory documentation, and cross-functional coordination to achieve site readiness and data integrity.

The position requires building strong site relationships, performing monitoring activities, and traveling up to 75% to support study sites globally.