Clinical Specialist

7 days ago


London, United Kingdom Hays Full time

Global Pharma specialising in rare disease is looking to recruit a contract Clinical Study Specialist to support the managers including oversight of site monitoring, site management and/or vendor management, and other activities as delegated by the Study Manager.

Excellent communication skills and previous clinical experience in the following

  • Study Management and Execution
  • Develop and/or review study specific documentation, as delegated by the Study Manager
  • Contribute to the management of country and site feasibility assessment
  • Contribute to the collection and oversight of essential documents for study life-cycle management
  • Contribute to the development of site and investigator training materials
  • May present at investigator meetings as assigned
  • Ensure timely study entry and updates to ClinicalTrials.gov
  • Ensure investigator payment: site set-up, pass-through processing, visit payment processing and funding processing (in collaboration with payment vendor)
  • Provide administrative assistance with internal and external meetings including investigator meeting(s) as warranted
  • Process documents for signature in DocuSign
  • Site management for delegated site(s)
  • Manage and resolve site related issues
  • Oversee the Clinical Trial Insurance process
  • Support Study Manager to ensure timely delivery
  • Support Vendor Management
  • Oversee and manage essential documents in the Trial Master File (TMF)
  • Contribute to Global Study Operations risks identification and mitigations.
  • Provide support and administrative assistance with internal and external meetings
  • Assist with filing GSO internal study documents in internal systems


Educated to degree level (science or nursing) and previous Clinical experience essential,

6 - 12 month contract hybrid role London

please contact me for further details


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