Job Details 
Phlexglobal
Our database has identified the following jobs as matching your search criteria. If you cannot see a job you are interested in, please search again refining your criteria or email us for further help and support.| Title | Clinical Trials Administrator | ||
|---|---|---|---|
| Role | Clinical Trial Administrator | Reference | RF/10630 |
| Location | Hertfordshire | Working hours | Full-time |
| Salary | On application | Employment type | Contract / Interim |
| Summary | Are you a committed and talented professional looking for a pivotal role in administration? Are you looking to break the mould and become a CTA with additional duties? We have a Clinical Trial Administrator role located in our client’s offices in Welwyn Garden City, Hertfordshire. This is a fantastic opportunity to expand your skills and knowledge by joining one of the principal pharmaceutical organisations. You will have the opportunity to work with a market leader, which has a continually growing pipeline of exciting products, enabling you build and develop your career path whilst working on a range of diverse and challenging products. This is your chance to contribute to the development of medicines for the global community. | ||
| Description | An opportunity to a pivotal part of a Clinical Research team. The CTA needs to be an organised, logical, enthusiastic and methodical worker with the will to succeed. You will be involved in most activities of the clinical trial required to set-up, conduct and complete ensuring you work to ICH GCP and company SOPs including: - Creation of study start-up tools, - Assisting in the ordering/distribution of study-related supplies and/or coordinating local suppliers and vendors - Assisting with ethics and/or health authority filing through the creation of necessary supportive documentation - Tracking of site contract approvals, invoices and payments - Reconciling/tracking essential documents necessary for the country-level TMF - Understand the role of the SAE Responsible and provides back-up or assumes full accountability - Co-ordinate and maintain contact lists - Meeting planning and execution - Develop and maintain functional knowledge of GCPs, company SOPs, local regulations and therapeutic area(s) - Co-monitor as required - Establish and maintain tracking systems/tools - Maintain country level TMFs in accordance with SOP requirements - Participate, as needed, in the development and distribution of newsletters for investigators and monitors - Assist with the oversight of the SUSAR reporting process | ||
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