On behalf of our Client - Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world, with more than 80 years of experience within the pharmaceutical and biotechnology industry a global pharmaceutical company - IQVIA is looking for a eTMF Specialist who can join an exciting working environment in a dynamic atmosphere.This position will oversee the global eTMF (electronic Trial Master File) operations for GRD R&D; including providing support to all study teams members involved in eTMF management.Responsible for creation and revision of all eTMF associated procedures, ensuring they are up to date and compliant with the applicable regulations.This position will assume the leadership role for global eTMF operation to ensure the quality KPIs are met and eTMFs are inspection ready at all times.Role:Global oversight of the eTMFs, ensuring that the study teams are maintaining inspection ready files across all programs.Establish KPIs and metrics for documents filed in the eTMF to improve performance, quality, risk mitigation and contingency planning.Develop and embed process excellence and consistency across eTMFs management.Establish industry standard processes for eTMF by incorporating the applicable changes to the TMF reference model.Accountable to ensure consistency in eTMF management at all stages (eTMF set-up, maintenance, QC/ QR and query management, final reconciliation, closure, migration and archiving).Provide TMF support for both inspection and audit activities for internal and external hosted audits.This includes working directly with Agency Inspectors (FDA, EMA, PMDA, MHRA, etc) or auditors; assist with retrieving documents, speaking to the TMF process and assisting with resolving potential issues identified.Responsibilities:70% - TMF Management and Reporting : Handles and maintains electronic TMF and electronic internal repository according to ICH/GCP guidelines and applicable regulations/ standards.Responsible for preparing the periodic intern