On behalf of our Client a global pharmaceutical company, IQVIA is looking for a eTMF Specialist who can join an exciting working environment in a dynamic atmosphere. JOB DESCRIPTION: -To ensure data management and statistics trial documentation is managed according to internal standards and regulatory requirements; -To oversee activities to ensure TMF documentation is published in a timely manner and with high quality in order to maintain TMF in an inspection and au-dit readiness; -To lead the Documentation and Data Archiving team providing subject matter expertise and guidance to team members; -To ensure providers match performance expectations; -To promote optimal use of tools and metrics related to documentation management. RESPONSIBILITIES: -To lead the documentation and data archiving team, recruiting, mentoring and developing the team; -To train DM/STAT CRO on Company standards and TMF related activity; -To monitor TMF related activities using metrics to evaluate status and gaps to ensure quality and timelines and evaluate corrective actions; -To support team members in the TMF plan activities and quality checks; -To participate to audit and inspection to TMF; -To perform regular checks on data archiving activities to ensure timelines are respected; -To contribute to eTMF process improvement and internal system development. REQUIREMENTS AND SKILLS. -Scientific degree; -A significant experience in a similar job in the industry or CRO; -Knowledge of drug development process; -Solid knowledge of clinical data management and statistical process and related documentation, standards and tools; -Strong knowledge of international standards for Trial Master File (TMF Reference Model); -Knowledge of ICH GCP and regulatory requirements with specific reference to data integrity, data archiving and document management; -Good knowledge of SAS System; -Knowledge of international data standards (CDISC) and regulatory requirements for data submission; -Project and budget management; -English knowledge; -eTMF - EDMS - SAS System. TYPE OF CONTRACT: Maternity replacement Chemical contract IQVIA reserves the right to evaluate candidates with domicile / residence and work experience / study with requirements responding to the open request. Applications WITHOUT the requirements Will NOT be fully taken into account. Please enter the authorization for the processing of personal data (DL196/2003) - General Data Protection Regulation (13 GDPR 679/16 –) to IQVIA and to transfer those data to IQVIA’s Clients. The research is urgent and is intended for candidates of both sexes (L.903/77). \#LI-CES #LI-DNP IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled