Trial Delivery Specialist - Clinical Trial Coordination
Core
Execution-focused role driving collaboration across internal and external partners to ensure operational excellence in clinical study management across all phases and therapeutic areas.
Role type
Senior IC clinical trial coordination specialist
Builds
Efficient, high-quality study delivery throughout the study life cycle
Domain
Biopharmaceuticals / Clinical Trials
Deliverable
client delivery
Required skills
risk identification and escalation, end-to-end operational study delivery, clinical document review, study plan development, cross-functional team coordination, country oversight, vendor and CRO management, clinical supply chain oversight, eTMF data oversight, budget and financial management
Preferred skills
none stated
Technologies
internal systems/databases/tracking tools
Responsibilities
Monitor study conduct and progress to identify and resolve risks; manage end-to-end operational study delivery from setup to archival; review clinical documents and support study plan development; coordinate study-related activities and cross-functional team communication; facilitate communication with internal and external stakeholders; oversee country activities including recruitment, data completeness, and compliance; manage vendor and CRO oversight; oversee delivery of clinical supplies and study materials; ensure eTMF completeness and inspection readiness; manage budget and financial activities
