Manager leading central monitoring activities for global studies at Fortrea. Transforming clinical trials with data and analytics to proactively manage risk and protect patients.
Responsibilities
Lead and execute central monitoring activities (site, subject, and study level) across multiple trials
Proactively identify risks using dashboards, analytics, and data review—and recommend mitigations
Manage a portfolio of studies and act as a key customer point of contact
Support study start‑up, risk planning, site risk assessments, and monitoring strategies
Collaborate on proposals, bid defenses, and sponsor presentations
Coach and mentor teams; contribute to process improvement and SOP development
Line manage and develop central monitoring staff
Requirements
5-7 or 7–9+ years of clinical research experience (CRO, pharma, or equivalent)
Strong knowledge of drug development and clinical trial execution
Experience in clinical monitoring, project management, data management, or analytics
University degree (Life Sciences preferred; equivalent experience considered)
Benefits
High‑impact, visible role in modern, data‑driven monitoring
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