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):
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Fortrea is a leading global contract research organization (CRO) specializing in clinical development solutions for pharmaceutical, biotechnology, and medical device companies. With over 19,000 employees operating in more than 90 countries, Fortrea provides comprehensive services across clinical development, patient access, and technology spanning more than 20 therapeutic areas. The company serves over 90% of the world's top 20 pharmaceutical companies, helping to advance drug and medical device development globally. Fortrea combines decades of experience in clinical development with a commitment to scientific precision and innovation.
