Local CTM - Finland - FSP
Core
Manage clinical operational and quality aspects of low to moderate complexity studies to ensure final clean data deliverables within contractual timelines.
Role type
Local Clinical Trial Manager (IC)
Builds
Clinical deliverables (clean data) for pharmaceutical/biotech customers
Domain
Clinical Research / Life Sciences
Deliverable
production ML models | product features | dashboards & analysis | client delivery
Required skills
Clinical monitoring, ICH GCP compliance, resource management, budgeting, regulatory submissions, team leadership, project tracking
Preferred skills
Clinical Study Manager (CSM) responsibilities, Accompanied Field Visits (AFVs), CRF design, ethics committee coordination
Technologies
Outlook, Excel, Word, automated clinical systems
Responsibilities
Manage clinical operational and quality aspects of allocated studies; Develop clinical tools (Monitoring Plan, Guidelines) 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; Lead team meetings and implement standardized monitoring processes
Seniority
Mid-Senior, hands-on IC
