Clinical Trial Associate

3 weeks ago

London, United Kingdom Labcorp Full time

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 with Good 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:
**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

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