Main Responsibilities
- The Central Monitoring Specialist is responsible for the execution of key Central Monitoring (Site, subject & study level review as applicable) activities and in assisting the execution of several key activities.
- The Central Monitoring Specialist collaborates with the study team to execute Central Monitoring and comply with the applicable plans for the study.
- Central Monitoring Specialist conducts review of the applicable Informatics platform and communicates findings at the country, study, site, subject level. He/she is responsible for the conduct of central monitoring activities in a timely manner and reporting, recommending changes in risk profile, and escalation as appropriate.
- He/she may conduct risk assessments, review risk indicators, recommend mitigations to project teams.
- Deep dive into identifying site & subject level risk in non-contributing RI which may overall affect the study level risk.
Qualifications(Minimum Required):
- University / college degree (life science preferred) from an appropriately accredited institution.
- Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
Experience (Minimum Required):
- Minimum of 3-5 years of relevant clinical research experience in a pharmaceutical company/CRO or other equivalent experience with increasing levels of responsibility in clinical trial related roles e.g., project management, clinical monitoring, data management and informatics.
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