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.