Senior Clinical Trials Coordinator
Core
Central coordination and delivery of investigator-initiated multi-site clinical trials from initiation to completion.
Role type
Senior Clinical Trials Coordinator
Builds
High-quality multi-site studies across the trial lifecycle
Domain
Clinical research / Healthcare
Required skills
Clinical trial coordination, multi-centre trial management, ICH-GCP compliance, ethics and governance submissions, project planning, participant recruitment support, budget tracking, financial management, data integrity, regulatory requirements knowledge, clinical trial management systems proficiency
Preferred skills
Tertiary qualifications in Health, Science, or Project Management, professional certification in Health or Project Management
Technologies
Clinical trial management systems, platforms and tools
Responsibilities
Coordinate and maintain project plans, agreements and essential trial documentation including ethics and governance submissions, study protocols, case report forms and trial master files; Support multi-site trial start-up, site initiation and monitoring activities maintaining audit-ready documentation; Monitor project milestones and contribute to participant recruitment, consent, data collection, budget tracking, financial management, pre-award activities and trial reporting; Build effective relationships with investigators, trial sites, collaborators and other stakeholders
Seniority
Senior, hands-on IC