Senior Ophthalmology CRA – Remote with Travel

Fortrea; Town of King (WI); A distancia; USD 130.000 - 142.000; Jornada completa

Descripción de la vacante

Fortrea is seeking Sr. CRAs with ophthalmology expertise to monitor clinical trials, manage site visits, ensure data integrity, and uphold regulatory compliance. You will use clinical judgment to safeguard participant safety and study quality in a fast-paced environment.

The role requires 3+ years of monitoring experience, travel 30-50% (overnight), and the ability to coordinate with vendors and sites. Remote-friendly options are available within the United States.

Formación

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

Responsabilidades

• Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -
• Responsible for all aspects of site management as prescribed in the project plans
• General On-Site Monitoring
• Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
• Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
• Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data
• Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested
• Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs
• Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management
• Assist with training of new employees, eg. co-monitoring
• Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned
• Perform other duties as assigned by management

Conocimientos

Ophthalmology expertise

Clinical Monitoring

Educación

Bachelor's degree in related allied health

Descripción del empleo

Fortrea is seeking Sr. CRAs with ophthalmology expertise to monitor clinical trials, manage site visits, ensure data integrity, and uphold regulatory compliance. You will use clinical judgment to safeguard participant safety and study quality in a fast-paced environment.

The role requires 3+ years of monitoring experience, travel 30-50% (overnight), and the ability to coordinate with vendors and sites. Remote-friendly options are available within the United States.