The CompanyOur client is a global group that produces and commercialises innovative medicines in respiratory, neonatology, rare disease and special care areas.ResponsibilitiesThe Clinical Trials Administrator will support the project team in the day-to-day activities ofstudies. Will liaise with both internal and external stakeholders as applicable on assignedresponsibilities.Assist the project manager and project team with tracking of project progress, adherence to deliverables and timelines.Assist with maintenance of the project timelineAssist in the preparation, handling, filing and archiving of clinical documentation and reportsPerform periodic reviews of study files to assess documentation completeness and resolution of issue to support inspection readiness statusLiaises with the CRO and vendors as applicable to track and monitor progress of activities and adherence to project scope and deliverablesSupport the project reporting with development of regular reports, newsletters and trackersSupport project meetings including scheduling and managing meetings with agendas and minutesProvide general project administrative supportExperienceBSc in life science or related fieldBasic knowledge of clinical research regulatory requirements i.e. GCP guidelinesComputer skills including working knowledge of Microsoft Word, Excel and PowerpointEffective time management and organizational skillsExcellent attention to detailExcellent written and verbal communication skills including English fluencyTo discover more about this opportunity please apply online or contact Darragh on for a confidential discussion.