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Guerbet is a leader in medical imaging worldwide, offering a wide range of pharmaceutical products, medical devices, digital and AI solutions for diagnostic and interventional imaging, to improve the diagnosis and treatment of patients.

A pioneer since more than 90 years in the field of contrast media, Guerbet is continuously innovating with 9% of revenue dedicated to Research & Development and four centers in France, Israel and the United States.

Guerbet (GBT) is listed on Euronext Paris (segment B – mid caps) and generated €817 million in revenue in 2019 with a global workforce of over 2,800 employees.

Achieve, Cooperate, Care and Innovate are the values that Guerbet's employees share and practice every day. Working at Guerbet means playing a unique part in the future of medical imaging. Passionate about its business, the company strive day in, day out to combine performance, quality and sustainable development.

For more information about Guerbet, please go to  and follow Guerbet on Twitter @GuerbetGroup


Medical Manager

    Responsible for all matters related to Medical affairs
    Provides accurate clinical and technical information for products.
    Develop/execute Japan medical strategy/ medical plan for DI (Diagnostic Imaging), II (Interventional Imaging) and AI (Artificial Intelligence)   as a member of Medical Affairs 
    Ensures valid answers are provided to medical information enquiries (MIEs) about the products using the available MI systems, processes and resources.
    Management of all Medical Information activities including responding to customer requests, producing scientific/educational materials and overall management of the Call Center.
    Provides medical review / approval of promotional materials for detailing/scientific aids (printed/digital/slide deck) scientific meetings, symposia and other medical educational activities in accordance to applicable codes of practice and regulations.
    Assists in the development of new claims for key brands
    Assists in defense of key claims when challenged.
    Assists in writing and amending SPC, PI and other relevant documents
    Provides scientific trainings
    Develop and Execute Medical activities/events aligned to Medical affairs plan 
    Assists in facilitating local evidence generation activities/ IIS as applicable. 
    Contributes to new product development and launch.  
    Coordinate and Support Medical Clinical Operations/Trials in Japan
    Engages KOL/Thought Leaders and external stakeholders through scientific communications.
    Manages the Grants office to assure efficient utilization of resources in support of academic/scientific activities.