| You will join a major global Contract Research Organisation (CRO), providing administrative and logistical support to the local Study Team (including Project Manager, CRAs and external service providers) responsible for delivering clinical trials in line with Good Clinical Practice (GCP) and relevant SOPs. Your duties as Clinical Trial Administrator (CTA) will include: - Co-ordinate the distribution and retrieval of clinical trial documentation, maintaining accurate document tracking and filing systems in line with GCP
- Act as central point of communication for the Study Team, investigator sites and vendors such as shipping and printing companies
- Organise and facilitate Study Team meetings, Investigator meetings, teleconferences etc. taking minutes and co-ordinating follow-up actions as required
- Assist the Project Manager in tracking study budgets, producing budget tracking reports as necessary and ensuring that payments are processed in a timely manner.
You should be a strong team player with the well-developed communication and interpersonal skills required to interact effectively with remote colleagues and service providers in a highly multicultural environment. You must be able to demonstrate an understanding of the principles of GCP relating to clinical study administration gained from first-hand experience of supporting clinical trials.You should be highly self-motivated and proactive in order to be comfortable and effective when working from home with minimal supervision. All candidates must be fluent in English AND either French or Dutch, and be authorised to work in Belgium. |
