Senior Ophthalmology CRA — Remote with Travel

Fortrea; Seattle (WA); Remote; USD 130,000 - 142,000; Full time

Job summary

Fortrea is seeking an experienced Senior CRA with ophthalmology monitoring expertise to join our FSP team. The role requires 3+ years of clinical monitoring experience and 30-50% overnight travel across major hub locations in CA, TX, and the US East and South regions.

Responsibilities include on-site monitoring, study file maintenance, regulatory compliance, data quality checks, SAE processing, and potential local project coordination.

Qualifications

• University or college degree, or certification in a related allied health profession (e.g. nursing licensure).
• 3+ years of Clinical Monitoring experience.
• 30-50+% overnight travel.
• Ophthalmology experience.

Responsibilities

• Oversee all aspects of site monitoring: routine monitoring, site close-out, study file maintenance, and initiation visits; liaise with vendors.
• Ensure proper entry of patients into the protocol and adherence to regulatory requirements during visits.
• Verify informed consent procedures and protocol requirements.
• Monitor data quality in CRFs or other data collection tools and query resolution.
• Manage registry activities and perform feasibility work when required.
• Complete SAE reporting and follow-up with narratives and reconciliation.
• CRF review and data review guidance adherence per project standards.
• Support training of new staff and co-monitoring when needed.
• Coordinate clinical projects as Local Project Coordinator and serve as local client contact if assigned.

Skills

Clinical Monitoring

Ophthalmology experience

Study coordination

Education

Bachelor's degree or allied health certification

Job description

Fortrea is seeking an experienced Senior CRA with ophthalmology monitoring expertise to join our FSP team. The role requires 3+ years of clinical monitoring experience and 30-50% overnight travel across major hub locations in CA, TX, and the US East and South regions.

Responsibilities include on-site monitoring, study file maintenance, regulatory compliance, data quality checks, SAE processing, and potential local project coordination.