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Research Support Ltd.

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Vendor Management/CRO Supervision > Project Management > Medical Writing > Clinical Trial Monitoring >  
Project Management

  • Managing clinical trials for sponsors or CROs, including as an interim solution.
  • Managing trials from study start-up to close-out.
  • I am accustomed to planning work, assigning and confirming ownership of tasks, regularly summarising project status, documenting decisions and following-up to ensure timelines are met by cross-functional project teams.
  • Where practical, I have performed the dual role of Project Manager and Monitor and have found this to be an advantage to anticipating and understanding site-level issues. For this reason I always recommend co-monitoring by the Project Manager.