The Company
Our client is a global group that produces and commercialises innovative medicines in respiratory, neonatology, rare disease and special care areas.
Responsibilities
The Clinical Trials Administrator will support the project team in the day-to-day activities of
studies. Will liaise with both internal and external stakeholders as applicable on assigned
responsibilities.Assist the project manager and project team with tracking of project progress, adherence to deliverables and timelines.
* Assist with maintenance of the project timeline
* Assist in the preparation, handling, filing and archiving of clinical documentation and reports
* Perform periodic reviews of study files to assess documentation completeness and resolution of issue to support inspection readiness status
* Liaises with the CRO and vendors as applicable to track and monitor progress of activities and adherence to project scope and deliverables
* Support the project reporting with development of regular reports, newsletters and trackers
* Support project meetings including scheduling and managing meetings with agendas and minutes
* Provide general project administrative support
Experience
* BSc in life science or related field
* Basic knowledge of clinical research regulatory requirements i.e. GCP guidelines
* Computer skills including working knowledge of Microsoft Word, Excel and Powerpoint
* Effective time management and organizational skills
* Excellent attention to detail
* Excellent written and verbal communication skills including English fluency
To discover more about this opportunity please apply online or contact Darragh on for a confidential discussion.