Senior CRA Ophthalmology - Remote + Travel

Fortrea; Minneota (MN); Teletrabalho; USD 130 000 - 142 000; Tempo integral

Resumo da oferta

Fortrea is seeking a Sr. Clinical Research Associate with ophthalmology expertise to monitor trial sites across the United States, ensuring protocol compliance and safeguarding participant welfare.

You will perform site visits, ensure proper training, and manage data quality while collaborating with vendors and study teams. The role requires 3+ years of experience and willingness to travel 30–50% overnight.

Qualificações

• 3+ years of Clinical Monitoring experience.
• Ophthalmology experience.
• Willing to travel 30–50% overnight.

Responsabilidades

• Responsible for all aspects of 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

Conhecimentos

Clinical Monitoring

Ophthalmology experience

Teamwork and communication

Overnight travel

Formação académica

Bachelor's degree or allied health certification

Descrição da oferta de emprego

Fortrea is seeking a Sr. Clinical Research Associate with ophthalmology expertise to monitor trial sites across the United States, ensuring protocol compliance and safeguarding participant welfare.

You will perform site visits, ensure proper training, and manage data quality while collaborating with vendors and study teams. The role requires 3+ years of experience and willingness to travel 30–50% overnight.