Senior Ophthalmology CRA – Remote (East Coast)

Fortrea; Virginia; Remoto; USD 125.000 - 142.000; Tempo pieno

Descrizione del lavoro

Fortrea seeks an Ophthalmology Sr. CRA to monitor clinical sites along the East Coast with 4+ years of monitoring experience. This full-time role offers remote options and requires strong clinical judgment and site management skills.

You will conduct site visits, ensure protocol adherence, manage SAE reporting, and coordinate data collection while travel occurs 30-50%. Oncology experience in early-phase trials is preferred, with duties spanning vendor liaison and regulatory compliance.

Competenze

• University or college degree, or certification in a related allied health profession.
• 5+ years of Clinical Monitoring experience.
• Oncology experience, early phase preferred.
• 30-50% overnight travel.

Mansioni

• Monitor all aspects of study sites, perform routine monitoring, initiate visits, and manage study files.
• Liaise with vendors and support site management per project plans.
• Conduct general on-site monitoring and ensure proper materials for protocol entry.
• Verify informed consent procedures and protocol adherence per regulations.
• Ensure data integrity on CRFs and monitor data quality.
• Oversee registry management and perform feasibility tasks as requested.
• Complete SAE reporting and narrative follow-ups per guidelines.
• CRF review, queries, and resolution per data management standards.
• Assist training of new staff and co-monitoring when needed.
• Coordinate projects as Local Project Coordinator and act as local client contact.

Conoscenze

Clinical Monitoring

Oncology experience

Site Management

Regulatory compliance

Formazione

University or college degree or allied health certification

Descrizione del lavoro

Fortrea seeks an Ophthalmology Sr. CRA to monitor clinical sites along the East Coast with 4+ years of monitoring experience. This full-time role offers remote options and requires strong clinical judgment and site management skills.

You will conduct site visits, ensure protocol adherence, manage SAE reporting, and coordinate data collection while travel occurs 30-50%. Oncology experience in early-phase trials is preferred, with duties spanning vendor liaison and regulatory compliance.