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Responsibilities 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 study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visi

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 initi

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 visi

Responsibilities 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 -…

Responsibilities Maintain awareness of regulatory legislation, guidance, and practice in the assigned countries Coordinate, collect and organize data and information required by EC/IRB/Third body/Regulatory Authority including but not limited to the…

Fortrea is seeking a Clinical Research Associate II to support Phase I clinical trials. The role includes monitoring and managing study sites, protecting participant safety, ensuring data integrity, and coordinating clinical project activities.

Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study fi

Responsibilities 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 -…

Responsibilities 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 -…

Fortrea Clinical Research Unit Inc. is hiring a Clinical Research Technician II to perform practical and administrative activities for Clinical Pharmacology trials in accordance with protocols and regulatory requirements.

Fortrea is seeking Clinical Trial Managers to oversee clinical delivery and operational activities for clinical research trials.

Fortrea is a global contract research organization providing clinical development, patient access, and technology solutions across multiple therapeutic areas.

Responsibilities Train new employees Routinely liaise with the Recruitment Supervisor, Screening Supervisor, Physicians and Study/Project Managers Backup for Clinical Pharmacology Recruitment SharePoint and liaison with call center Setup studies in…

Fortrea is hiring Clinical Research Associates through its Monitoring Excellence Academy for oncology, CAR T, and ophthalmology clinical trials.

Responsibilities End-to-end oversight of start-up and clinical responsibilities—from site identification through to database lock—through proactive management of project scope, timelines, milestones, and budget Ensure start-up and clinical project plans…

Fortrea is a clinical research organization providing clinical trial services to sponsors. The company is seeking Clinical Research Associates to monitor oncology or CAR-T studies, manage study sites and registries, ensure participant protection and data…