[Hiring] Senior Central Monitoring Specialist @Fortrea

Role Description

The Central Monitoring Specialist is responsible for the execution of key Central Monitoring activities and assisting in several key activities. The role includes:

• Collaborating with the study team to execute Central Monitoring and comply with applicable plans for the study.
• Conducting review of the applicable Informatics platform and communicating findings at the country, study, site, and subject level.
• Conducting central monitoring activities in a timely manner and reporting, recommending changes in risk profile, and escalation as appropriate.
• Conducting risk assessments, reviewing risk indicators, and recommending mitigations to project teams.
• Identifying site and subject level risk in non-contributing RI that may affect the overall study level risk.

Qualifications

• University / college degree from an appropriately accredited institution.
• Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Requirements

• Minimum of 6 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).

Company Description