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