Global Clinical Trial Manager II or Senior, Home based Poland
Core
Manage all aspects of Phase 1-4 clinical research studies, overseeing site management, clinical monitoring, and central monitoring deliverables to ensure patient safety, protocol compliance, and data integrity.
Role type
Senior Clinical Trial Manager
Builds
Clinical trial operations and monitoring deliverables for life sciences clients
Domain
Life Sciences / Clinical Research
Required skills
Clinical trial management, site management oversight, clinical monitoring, central monitoring, risk assessment, budget management, protocol execution, stakeholder communication, regulatory compliance (GCP), data integrity management, resource allocation, system oversight (CTMS, EDC, TMF)
Preferred skills
Strategic thinking, problem-solving, training coordination, conflict resolution
Technologies
CTMS, EDC, eDiary, ePROs, TMF, IVRS/IWRS, Central Monitoring dashboards
Responsibilities
Oversee site interactions post-activation through closeout including patient recruitment and investigator payments; Identify critical data and process risks using RACT; Review study scope, budget, and protocol content; Escalate risks to project managers; Participate in key meetings like Kick Off; Serve as escalation point for investigator communications; Collaborate with functional leaders for delivery handoffs; Develop and maintain clinical study tools and templates; Coordinate training for the study team; Oversee resourcing allocations for CRAs and Central Monitors; Review project oversight dashboards and clinical trial systems; Review content and quality of monitoring documentation.
Seniority
Senior, hands-on IC with management oversight