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Chris King posted a job: Clinical Trial Administrator - UK "Clinical Trial Administrator - UK Summary of Position: Administer, maintain and co-ordinate the logistical aspects of clinical trials in compliance with Good Clinical Practice (GCP) and relevant Standard Operating Procedures (SOPs). Primary Roles & Responsibilities: Arranging & participating in the organisation of Investigator Meetings & Study Team Meetings. Taking minutes & distributing. Assist with the Ethics / Regulatory Submissions; keep a track of submissions & approvals for the study. Preparing Protocols, Investigator Brochures and CRFs which includes keeping track and re-ordering supplies. Set up and maintenance of the Trial Master Files (TMF) or Electronic filing systems/ set up of the Investigator Site File (ISF) Managing and maintaining study documents & trial supplies e.g.; Patient Information Sheets, Patient Diaries, Lab Kits & Medical equipment for sites. Preparing essential clinical trial documentation, distributing, tracking and filing of documents on return. Ensure that any clinical trial databases/ tracking tools are set up and maintained throughout the trial. For more details please call Chris King on 01293 776644 or email cking@barringtonjames.com" |
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Thursday, October 13, 2011
New job Clinical Trial Administrator - UK
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