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 Assistant | ||
|---|---|---|---|
| Role | Clinical Trial Administrator | Reference | RF10676 |
| Location | Surrey | Working hours | Full-time |
| Salary | On application | Employment type | Contract / Interim |
| Summary | Clinical Trials Administrator Assistant – Surrey – Entry Level Role Are you looking for an entry level role into the Clinical Research Industry? We have a Clinical Trial Administrator Assistant role located in our client’s office in Surrey. Our client is one of the principal Pharmaceutical organisations and 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 be a pivotal part of a Clinical Research team. The CTA Assistant needs to be an organised, logical, enthusiastic and methodical worker with the will to succeed. Responsibilities will include: - supporting a team of field-based managers - providing support to the CTA team - diary management - taking minutes at meetings - arranging travel - typing reports and letters - ad hoc administration duties The successful candidate should come with a strong administrative background. You should be fully competent in the use of word-processing and the use of Microsoft Office. You should be a confident communicator as you will be required to liaise with work colleagues at all levels. Flexibility and the ability to work under pressure with minimum supervision would be a key advantage as would a working knowledge of clinical research and familiarity with ICH GCP, however, this is not essential. The CTA Assistant role gives you the unique opportunity as an administrator and as a member of the Clinical Trials team to be involved in a variety of aspects of the clinical trial process. All applicants must be eligible to work in the UK. | ||
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