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Clinical Trial Administrator Consultant
Apply locations Bologna time type Full time posted on Posted Yesterday job requisition id JR000126Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.
Job Description Summary
The Clinical Trial Administrator Consultant will manage and review the study documents of Clinical TrialsJob Description
Study documentation and Trial Master File (TMF):
- Responsible for reviewing the paper TMF (all Zones of DIA Ref.Model) of some closed studies, including the check of the completeness of the TMF, the quality of the documentation and the correctness of the TMF location. ,
- Responsible for TMF and paper TMF reconciliation after study completion
- Be involved in TMF inspections
- Manage NDA Filing
- Collaborates with the CPM with corrective and preventive actions, in case of deviations and audits.
Requirements:
- at least 3 years of experience in a Clinical Trial Assistant/Clinical Trial Administrator/Clinical Trial Coordinator/TMF Specialist position
- Fluent in English
- willing to be commuted to Parma office everyday
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