Clinical Trial Administrator - not your Usual CTA role

A global pharmaceutical company, who has major influence within the industry, is seeking an experienced clinical trial administrator (CTA) to join their team in London. Their European division is rapidly growing and this could be the chance for you to be part of a team who makes a difference within the pharmaceutical industry.

You will be working along side the study manager to support the management of clinical studies and associated operational activities in accordance with country-specific regulations, ICH Guidelines, Good Clinical Practices (GCPs), and the company's standard operating procedures (SOPs) and business processes. You will act as a key contact for CROs and internal study team members for the collection and management of regulatory documents.

You will need to have a minimum of 18 months as a CTA within clinical operations and have study start up and close experience in at least one study. In addition, you will need to have experience of developing new systems and processes and the application of scientific/medical and clinical concepts used to conduct a clinical trial.

For a confidential discussion call me on asking for Jonathan Garzon. To apply now send your CV in a word format to

Key words: CTA, Clinical Trial Administrator CTA, Clinical Trial Associate, Clinical Study Specialist, Clinical Study Technician, Clinical Operations Assistant, Administration, Trial Master File, TMF, Electronic Trial Master File, eTMF, Good Clinical Practice, ICH GCP, Case Report Forms, SOP, R&D, London, UK