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CTA role within global Pharma R&D team on M4/M40 corridor available on CSL Permanent Headcount or on contract working full-time.

Join a progressive and innovative company and enable their global study managers to deliver excellence. You will need^to be experienced in GCP study administration already and want to contribute to ensuring compliance for global trials in Phases I-IV. The scope of role is significant and varied; you will have the option of some travel, be involved with team liaison^and meetings, track and plan agendas and finance and liaise with third parties outside the company and within affiliates.

These CTA roles work beyond UK boundaries and demand immediate competence in WORD/Excel and knowledge of PowerPoint. The roles have flextime access and you will work in a highly motivated, credible company where you will be treated as an integral and valued team member on assignment. This is specialist CTA position providing support to the GCP Manager and Compliance Officer both based in the UK.

We would like the candidate to have a strong background of working in clinical research in the industry and be familiar with ICH GCP & national regulatory requirements.