On behalf of my client, a global pharmaceutical company we have a new vacancy for a Clinical Trials Administrator.
Reporting to the Head of Clinical Development you will be responsible for supporting the project team in the day-to-day activities of studies. You will liaise with both internal and external stakeholders as applicable on assigned responsibilities.
Role and 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
Qualifications & Experience required:
Essential
· 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
Desirable
· Clinical trial experience working with either CRO or Sponsor
· Experience working in a multidisciplinary team
For full details & discussion email your CV to [email protected] or call Tina at +353 1 2784701. Thornshaw Scientific is a division of the CPL Group. www.thornshaw.com