Hybrid Manager – Central Monitoring

Posted 38 minutes ago

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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

Manager – Central Monitoring

Job type

Experience level

JuniorMid level

Salary

Not specified

Degree requirement

Bachelor's Degree

Location requirements

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