eTMF Specialist

Zürich  ‐ Vor Ort
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Beschreibung

eTMF Specialist wanted for our Zurich based client in the pharmaceutical sector.

Your experience/skills:
  • Bachelor degree in life science, clinical research or equivalent
  • 5+ years' of clinical trial experience in the pharmaceutical industry and with electronic Trial Master File (eTMF)
  • Knowledge of TMF processes, related standards and quality control as well as understanding of ICH-GCP quality standards and other relevant regulations
  • Proficiency with Microsoft Office applications
  • Languages: fluent English both written and spoken


Your tasks:
  • Supporting development delivery functions with tasks related to the eTMF quality control
  • Providing guidance on the process according to the applicable SOPs, WIs, guidelines and eTMF management plan
  • Monitoring internal and vendor functions on the eTMF quality issues
  • Performing an ongoing quality control of the eTMF and ensuring its inspection readiness as well as reviewing eTMF management plans and provide relevant input
  • Providing support by eTMF related audit or inspections


Start: ASAP
Duration: 6MM+
Location: Zurich, Switzerland
Ref.Nr.: BH14006

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
Start
02/2019
Dauer
6 months
Von
RM Group
Eingestellt
25.01.2019
Projekt-ID:
1708366
Vertragsart
Freiberuflich
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