Centralized Clinical Trial Manager
Core
Reviewing clinical trial site visit reports to ensure quality, minimize errors, and escalate issues; acting as a liaison between monitoring and management teams.
Role type
Centralized Clinical Trial Manager
Builds
Clinical trial data quality and patient safety oversight
Domain
Healthcare / Clinical Research
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical trial data review, protocol deviation management, safety trend analysis, process improvement, project management, regulatory knowledge (ICH GCP)
Preferred skills
Advanced degree in life sciences, on-site monitoring experience
Technologies
OMR, ICO trial systems, Sponsor CTMS
Responsibilities
Review and approve visit reports per protocol and SOPs; follow up on action items and protocol deviations; observe and escalate patient safety trends; oversee quality metrics (MVR, FUL timelines); liaise with CTM and PMs for issue resolution; provide feedback on report quality trends.
Seniority
Manager, hands-on IC