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 CPA:

• 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.

Must Have

• Minimum qualifications posted above

• Basic understanding of GCP, ICH Guidelines and local regulations as they apply.

• Basic knowledge of the drug development process as it relates to the execution of clinical trials with a focus on document flow.

• Experience in managing multiple priorities and able to accomplish tasks within a timeframe, setting milestones to meet deadlines and to achieve goals.

• Demonstrates ability to function independently

• General knowledge of software systems and web-based applications. Good computer aptitude and willingness to learn new systems and applications.

Preferred

• Experience in the use of industry Clinical Trial Management Systems and Clinical Trial Master File Systems or equivalent

• Additional complex software application related to clinical trial research (i.e electronic data capture or patient diaries, interactive voice response, etc...)

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