Labcorp is looking for an experienced Clinical Trial Administrator in the South East of England to be client-dedicated with a prestigious Pharmaceutical company that has an outstanding reputation in the UK in terms of employee satisfaction. This opportunity is permanent,full time and part office (50%), part home based (50%).

For this particular role we are ideally looking for a 'career' clinical administrator who does not wish to progress to a CRA or Project Management role.

Overview:

To provide comprehensive support to the clinical project team for the set-up and administration of clinical trials ensuring adherence to protocols and quality of information received, in line withGood Clinical Practice (GCP) and company Corporate and Local Standard Operating Procedures (SOPs).

To achieve success it is critical for the CTA:

• To provide pro-active management of all administrative aspects of the set up and conduct of clinical trials.
• To provide administrative support and focal point of contact as defined above for the Regional/Local Clinical Project Leaders (CPL), Regional Trial Manager (RTM), Start-Up/Regulatory Team and a team of Clinical Research Associates.
• To prioritise and organise a varied workload for different team members who sometimes have conflicting priorities.

Required experience:

• Knowledge of and experience with GCP and other regulations in force; ability to learn and apply SOPs and quality control.
• Good IT skills in MS (Word, Excel, Powerpoint, Outlook) and other company applications are essential.

Other Information: This role is afull time & permanent position to beemployed through Labcorp. For more information please contact Andy Smith at Labcorp on +44 (0)7775 848 250 or email andy.smith@covance.com

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