Description
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.: BH11862
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