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About the role
- 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
- Global exposure and strong client interaction
- Collaborative culture with room to grow and lead
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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