Description:
This client-dedicated role is to be office based in central London for at least 2 days a week with the rest of the time being spent working from home OR 100% home based in Ireland. Ideally you will have at least 1-2 years experience of supporting Clinical Trials in the UK / Ireland. Much of the work will involve complex Oncological Clinical Trials and so there is plenty of interesting (and worth while) work to get your teeth stuck into!
Essential Job Duties:
- Act as contact for project team and study sites
- Perform CRF review against established data review guidelines, under direct supervision on management systems
- Assist with the management of study supplies and organize shipments
- Create, update, track, and maintain study-specific trial management files, tools, and systems.
- Assist the local project team members with other administrative activities as required (e.g. payments to investigators, correspondence with clients, preparation of status reports, and organization of investigators’ meetings)
- Coordinate meetings with clients, investigators, and project team, including taking minutes.
- Ensure compliance with Covance SOPs, FDA, ICH, and GCP regulations for clinical conduct in all aspects of daily work
- Provide input in writing Monitoring Conventions as assigned
- Assist in submissions and notifications to Ethics Committees and Regulatory Authorities
Requirements:
- a minimum of 12 months of Clinical Research Admin experience from a CRO or Pharma company - This is essential!
- You must live in commuting distance of Central London, again essential.
- Basic understanding of biology and biological processes
- Good organizational and time management skills