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Manage and monitor clinical study sites according to guidelines, ensuring data integrity, compliance, and efficient resource use while interacting with internal teams.

The Safety Systems Specialist II oversees safety system implementation, configuration, and support, ensuring quality service and collaboration with stakeholders while conducting data analysis and training.

Manage clinical safety operations, process adverse event reports, ensure regulatory compliance, and prepare safety summaries and reports. Support training and project management initiatives while maintaining quality standards.

The Senior Site Navigator coordinates site activities for clinical studies, ensuring compliance and efficient site activation, while mentoring junior staff and resolving potential study delays.

The Change Manager will support Clinical Data Management through coordinated change activities, working closely with project teams and stakeholders to ensure smooth adoption of changes and successful implementation of multiple transformation initiatives.

This role involves site management and monitoring for clinical studies, ensuring compliance with regulations, and maintaining data integrity during trials.

The Clinical Start-Up & Trial Lead oversees clinical trial activities from start to finish, ensuring operational excellence and managing stakeholder communications.

The Data Architect will design and implement ETL workflows, manage data integration strategies, and develop scalable data repositories to enhance drug development at Fortrea.

The Site Navigator II coordinates clinical study activities, ensures regulatory compliance, oversees site management, supports training, and communicates effectively with stakeholders while managing study milestones and compliance reviews.

Assist with safety system implementation and support, conduct configurations, develop reports, support users, and perform system testing and training.