TMF Repositories Support Lead

Apply nowLocations: Basel, Switzerland Full timeR1133232Date Posted: 06.20.2020

Job description

TMF Repositories Support Lead - Sponsor dedicated

As TMF Repositories Support Lead, you will act as business lead for integration and interfaces of TMF repositories and support improvements and innovation on business and technical aspects of document management and archiving, including implementation of innovative methods.

Your main responsibilities will include, but not limited to:

• Ensure as a Business lead that assigned systems/tools (e.g. VirtualTOC, eTMF4 etc) can support Clinical Trial Teams and inspector/auditor activities.


• Provide support before, during and after audits and inspections on questions related to TMF systems, tools and processes.


• Support the strategy for integration and/or interfaces of identified TMF repositories with the new Document Management System and assess future systems functionalities to ensure compliance with regulatory requirements.

1) Maintain and implement the plan for integration and or interfaces of identified TMF repositories into the new Document management System.

2) Ensure compliant storage of TMF documents/data in Novartis by developing and supervising trainings courses, migration procedures and processes.

3) Contribute to the implementation of global plan for archiving the electronic TMF documents authored/imported in the different Novartis Systems.

• Support future releases of new document management system by providing direct input to the user requirements, change requests, file plan, migration, testing and deployment


• Support enhancement of TMF documents/data access throughout the company and for inspections,


• Act as a Core member of the TMF Governance Team for any TMF related questions and supporting procedures, guidelines and tools update/creation.

What you’ll bring to the role:

• College degree or equivalent education in life science/healthcare or related scientific discipline (natural, pharmaceutical, medical, archival or information technology).


• Fluent English (oral and written)


• At least 5 years of relevant experiences in managing, archiving, retrieving or compiling clinical documents / At least 6 years of relevant clinical research/pharmaceutical industry experiences


• Lead Expert in electronic Trial Master File systems and Archiving


• Good organizational and IT skills and significant project work or project management experience Additional requirements:


• Experience with stakeholder management in a matrix organization.

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

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