Jobs at Syneos Health

Lead site management, clinical and central monitoring activities to ensure patient safety, protocol/GCP/regulatory compliance and data integrity. Oversee CRAs/Central Monitors, manage resourcing, review monitoring documentation, coordinate with cross-functional teams, identify and mitigate risks, maintain study tools/systems (CTMS/EDC/TMF), support budget oversight and training, and provide status updates to clients and leadership. Moderate travel (~20%) may be required.

Manage site oversight, clinical and central monitoring, and risk-based activities to ensure patient safety, protocol/GCP/regulatory compliance and data integrity. Coordinate cross-functional teams, oversee CRAs/central monitors, maintain study tools (CTMS/EDC/TMF), review monitoring documentation, escalate risks, support training and UAT, and drive study milestones including enrollment and database lock.

The CRA II- SCRA conducts site qualification and management activities, ensuring compliance with regulatory guidelines, supporting patient recruitment, and documenting site activities.

The CRA II- SCRA will oversee site activities, ensuring compliance with regulatory standards while performing monitoring, data verification, and site management throughout the study lifecycle.

Perform site monitoring, manage clinical data compliance, document activities, ensure regulatory compliance, support patient recruitment, and liaise with project teams.