Help shape the future of riskbased clinical trial oversight.
At Fortrea were transforming how clinical trials are monitoredusing data analytics and expert insight to proactively manage risk and protect patients. Were seeking a Manager or Associate Manager Central Monitoring to lead central monitoring activities across a portfolio of global studies and serve as a trusted partner to sponsors and project teams.
What Youll Do
- Lead and execute central monitoring activities (site subject and study level) across multiple trials
- Proactively identify risks using dashboards analytics and data reviewand recommend mitigations
- Manage a portfolio of studies and act as a key customer point of contact
- Support study startup 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
- (If applicable) Line manage and develop central monitoring staff
What You Bring
- 5- 7 or 79 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)
Why Fortrea
- Highimpact visible role in modern datadriven monitoring
- Global exposure and strong client interaction
- Collaborative culture with room to grow and lead
Apply now and help redefine how clinical trials are monitored.
Learn more about our EEO & Accommodations request here.
Required Experience:
Manager
Help shape the future of riskbased clinical trial oversight.At Fortrea were transforming how clinical trials are monitoredusing data analytics and expert insight to proactively manage risk and protect patients. Were seeking a Manager or Associate Manager Central Monitoring to lead central monitoring...
Help shape the future of riskbased clinical trial oversight.
At Fortrea were transforming how clinical trials are monitoredusing data analytics and expert insight to proactively manage risk and protect patients. Were seeking a Manager or Associate Manager Central Monitoring to lead central monitoring activities across a portfolio of global studies and serve as a trusted partner to sponsors and project teams.
What Youll Do
- Lead and execute central monitoring activities (site subject and study level) across multiple trials
- Proactively identify risks using dashboards analytics and data reviewand recommend mitigations
- Manage a portfolio of studies and act as a key customer point of contact
- Support study startup 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
- (If applicable) Line manage and develop central monitoring staff
What You Bring
- 5- 7 or 79 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)
Why Fortrea
- Highimpact visible role in modern datadriven monitoring
- Global exposure and strong client interaction
- Collaborative culture with room to grow and lead
Apply now and help redefine how clinical trials are monitored.
Learn more about our EEO & Accommodations request here.
Required Experience:
Manager
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