eTMF specialist wanted for our Zurich based client within the Pharmaceutical sector.

Your experience/skills:

  • Bachelor degree or equivalent, preferably in life science, clinical re- search, or related discipline.
  • Comprehensive practical knowledge of TMF processes, related standards (e.g. DIA Reference Model) and its quality control.
  • Thorough understanding of ICH-GCP quality standards and other relevant regulations
  • Minimum 5 years of clinical trial experience in the pharmaceutical industry or university hospital, with a minimum of 3 years’ experience with the eTMF.

Your tasks:

* Perform an ongoing quality control of the eTMF. Ensure its inspection readiness i.e. completeness and compliance with the relevant requirements from study start-up until archiving.
* Monitor the eTMF quality issues and follow up with the relevant functions (sponsor / vendor) until their resolution.
* Provide regular eTMF process guidance on the eTMF related
* Contribute to the revisions of the eTMF process and system enhancements.
* Perform review of the eTMF management plans and provide relevant input.
* Provide support by eTMF related audit or inspections.

Start: ASAP
Duration: 6 MM
Location: Zurich, Switzerland
Ref.Nr.: BH 14642

Does this sound like an interesting and challenging opportunity to you? Then take the next step by sending us your CV as a Word document and a contact telephone number.

Due to work permit restrictions we can unfortunately only consider applications from EU or Swiss citizens as well as current work-permit holders for Switzerland.

Going the extra mile…

New to Switzerland? In case of successful placement, we support you with:

  • All administrative questions
  • Finding an apartment
  • Health – and social insurance
  • Work permit and much more