Sr CTM / CTM - FSP
Core
Accountable for achieving final clinical deliverables (clean data from evaluable patients) within contractual timeframes for moderate to high complexity studies.
Role type
Senior Clinical Trial Manager (IC)
Builds
Clinical study data and regulatory-compliant documentation
Domain
Clinical Research / Life Sciences
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | physical/clinical work
Required skills
Clinical monitoring, ICH GCP compliance, resource management, budget forecasting, risk management, regulatory submissions, site communication, query resolution, team leadership
Preferred skills
Process improvement, regional lead responsibilities, financial acumen
Technologies
Outlook, Excel, Word, automated clinical systems
Responsibilities
Manage clinical operational and quality aspects of allocated studies; Develop clinical tools and Trial Master File sections; Monitor clinical activity timelines and metrics; Coordinate start-up activities and regulatory submissions; Communicate with study sites on protocol and data issues; Manage clinical resources and delegation.
Seniority
Senior, hands-on IC with potential for regional lead responsibilities
