CTM
Core
Accountable for achieving final clinical deliverables (clean data) within contractual timeframes for low to moderate complexity studies, ensuring quality, cost, and scope compliance.
Role type
Senior Clinical Trial Manager (IC)
Builds
Clinical trial operations and data deliverables for pharma/biotech clients
Domain
Clinical Research / Life Sciences
Deliverable
production ML models | product features | dashboards & analysis | client delivery
Required skills
Clinical monitoring, ICH GCP regulations, resource management, financial acumen, project planning, team leadership, regulatory submissions, CRF management, query resolution
Preferred skills
Clinical Study Manager (CSM) experience, Accompanied Field Visits (AFVs), bid defense preparation, Master Action Plan development
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; supervise clinical activity timelines and metrics; coordinate start-up activities and regulatory submissions; conduct field visits and monitor study performance; manage clinical resources and budgets.
Seniority
Senior, hands-on IC
