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 Project Associate | ||
|---|---|---|---|
| Role | Clinical Project Associate | Reference | CH10859 |
| Location | Working hours | Full-time | |
| Salary | £12,000 - £20,000 | Employment type | Permanent |
| Summary | Clinical Project Associate – Buckinghamshire Are you a committed and talented professional looking for your first pivotal role in clinical trial administration? Join our Task Force and let Phlexglobal assist you in realising your potential! | ||
| Description | We have a Clinical Project Associate (CPA) role within our Task Force team who are the industry’s hit-squad. Our Task Force team are involved with working on short-term contracts for clients for anything up to six months. You will be flexible, willing to travel across the country with the ability to provide full clinical and logistical project support to client companies. You will gain a huge range of exposure through working with pharmaceutical, CRO, biotech clients and the NHS. As a CPA you will need to be an organised, logical, enthusiastic and a methodical worker with the will to succeed. You will undertake an intense training programme to equip you with the necessary skills to have a successful career within clinical research. Once successfully completed 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: •Set up of TMF (Trial Master File) and ISF (Investigator Site File) on behalf of the client company, in accordance with the client company SOPs or Phlexglobal Ltd SOPs and ICH GCP. •Re-development/make suggestions to develop filing hierarchy; in accordance with generic/ Phlexglobal templates. • 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. •Compilation, copying, distribution and archiving of essential study documentation. •Scanning and indexing of client study documentation. •Provision of tracking logs and templates for client companies for use in ongoing studies/trials. | ||
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