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 (CTA) | ||
|---|---|---|---|
| Role | Clinical Trial Administrator | Reference | CH10860 |
| Location | Buckinghamshire | Working hours | Full-time |
| Salary | £20,001 - £30,000 | Employment type | Permanent |
| Summary | Experienced within Clinical Trial Administration and looking for a new challenge? We have exciting opportunities for Clinical Trials Administrators within our Task Force team which will offer you training and the career progression that you are looking for. Our Task Force department is a fast paced, dynamic team, are known as the industry "hit squad" and are involved in many varied projects enabling to gain a broad based experience of the pharmaceutical industry. You will be flexible, willing to travel with the ability to provide full clinical and logistical CTA support to client companies. You gain a huge range of exposure through working with pharmaceutical, CRO, biotech clients and the NHS. There is great scope for career progression! | ||
| Description | You will be working for numerous clients throughout the role so it's safe to say it will look excellent on your CV! You will also receive a car allowance, and you will get mileage paid when you are working at a client - having your own transport for this role is essential! The monitoring arm of Task Force is also growing rapidly and there will be scope for you to join this section of Task Force and to gain the training you need to begin your CRA career if this is the route you would like to take alternatively we are always looking for career CTAs to remain within our Task Force to grow your career. As a CTA you will need to be an organised, logical, enthusiastic and a 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, but not limited to: Pre Audit/Inspection review of TMF (Trial Master File) documentation in accordance with Phlexglobal Ltd or the client company SOPs. Undertaken either at the client company or at the offices of Phlexglobal Ltd. Set up of TMF and Investigator Site Files on behalf of the client company, in accordance with the client company SOPs or Phlexglobal Ltd SOPs and ICH GCP. Devising new filing structures as well as basic filing maintenance (electronic and hard copy). Set up and maintenance of electronic filing templates. Clearance of filing backlogs on behalf of a client company (electronic and hard copy). Subsidiary file management. TMF Copying, distribution and Archiving. Scanning and indexing of client study documentation. Provision of tracking logs and templates for client companies for use in ongoing studies/trials. Preparation of documentation for Archive, in accordance with Phlexglobal Ltd SOPs and industry standards. Writing, reviewing and working to Phlexglobal Ltd and client company SOPs and ICH GCP. Training and mentoring of staff of a client company and Phlexglobal Ltd employees in GCP documentation, archiving and filing. Other appropriate CTA duties as and when required. Ability to travel and work at client premises where required – occasionally for periods away from home. | ||
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