eTMF Specialist

On Application
27 Nov 2018
27 Dec 2018
Contract Type

eTMF Specialist – Switzerland

Job Responsibilities

  • Carry out routine quality control checks of the eMTF, including checking compliance with the relevant requirements
  • Report any limiting factors or elements of non-compliance to the appropriate functions, providing comprehensive solutions
  • Provide process guidance on requirements according to the applicable SOPs, WIs, guidelines, and eTMF management plan
  • Practically support eTMF users in using the system
  • Review the eTMF management plans and provide input
  • Arrange shipments of wet-ink documents

Key Skills

  • Strong problem-solving skills
  • Excellent time management and ability to simultaneously work on multiple projects
  • Proficiency with Microsoft Office applications, and experience using the electronic Trial Master File
  • Thorough understanding of ICH-GCP quality standards and other relevant regulations


  • BSc or equivalent, preferably in life science, clinical research or a related discipline
  • 5 years minimum clinical trial experience in the pharmaceutical industry or university hospital
  • 3 years minimum experience with the eTMF
  • Practical knowledge of TMF processes and related standards, and their quality control

Apply now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Hobson Prior is a leading specialist life science recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.


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