Director, Site Management & Monitoring (Clinical Research)
Core
Manage clinical research study delivery, team performance, and quality assurance for oncology trials at the country level.
Role type
Senior IC clinical research director (oncology)
Builds
Clinical research studies for oncology pipeline
Domain
Healthcare / Clinical Research / Oncology
Deliverable
production ML models | product features | dashboards & analysis | client delivery | infrastructure | physical/clinical work
Required skills
project management, line management, financial management, stakeholder management, analytical thinking, critical reasoning, presentation skills, communication, organizational skills, coaching, negotiation, planning
Preferred skills
oncology domain expertise, change management, quality improvement, eTMF management, forecasting
Technologies
MS Office, eTMF systems
Responsibilities
Manage change with a positive approach for self, team and business; Ensure adequate resources for the studies assigned; Development and performance management of direct reports; Contributes to efficient Clinical Research Department organization and its functioning at country level; Oversees successful delivery of Clinical Research study delivery country level targets to plan, with speed and quality; Ensures all systems are continuously updated; Ensures completeness and timeliness of the eTMF to maintain it "Inspection Ready"; Provides direction to LSADs/teams on major study commitments including resolving any key issues identified; Performs accompanied site visits/co-monitoring visits/training visits/QC visits according to local QC Plan, supporting ongoing coaching and development.
