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 | RF10479 |
| Location | Middlesex | Working hours | Full-time |
| Salary | £20,001 - £30,000 | Employment type | Permanent |
| Summary | A global pharmaceutical company, headquartered in Japan that employs just under 14,000 people worldwide is looking for an experienced CTA to join their existing team in Staines. | ||
| Description | The main purpose of this position is to work within ICH-GCP guidelines and company SOP’s, whilst providing administrative support for all company sponsored clinical trials. To enable this to be carried out to the required level an understanding and previous exposure within a clinical trials environment is essential. Day to day core tasks and responsibilities ate to include but not be limited to; • Set up and maintenance of electronic and paper filing including TMF Management in accordance with company SOP’s • Track and log essential trial documents • Keep Clinical Trials database up to date according to SOP’s. • Distribute study documents to affiliates • Raise cheques and maintain records of payments for each study • Archive completed studies; support review of files for essential documentation • Audit preparation • General secretarial duties, including letter writing and travel arrangements • Assist in organisation of departmental meetings • Training document coordination • Any addition admin duties as required. This is a demanding role that will need an organised and proactive team player. A good working knowledge of the internet, Microsoft Office and Outlook packages is essential. You must have high attention to detail and be able to prioritise a busy workload. Previous knowledge of ICH GCP and current clinical trial legislation is essential as is an understanding of the ethics approval process for the clinical trial process. In return this forward thinking and progressive organisation can offer a competitive basic salary and an excellent benefits package to include 25 days holiday, private medical healthcare, dental plan, life assurance, income protection, reduced gym membership, staff restaurant and onsite parking. If you have the relevant background and are looking for a new challenge then please do not delay in attaching you CV for the opportunity of an immediate interview. If you have the desire, skills and tenacity to succeed within the Clinical Trials field then contact the Phlexglobal Resourcing team. | ||
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