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Hugo SohierHS

Hugo Sohier

Audiologist - MedTech Consultant

€750/day
3 projects
Paris, FR
3-7 years

Average response time: 2 hours

Freelancer profile translated to English.
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About Hugo

Graduated in audioprosthetics and holder of a master's degree in sensory and motor neuroprosthetics, I have been working in the healthcare sector for several years.

My professional experiences and the development of my skills in the field in France and abroad have allowed me to hold the position of Clinical and Technical Manager for the world leader in cochlear implants for several years.

I was able to acquire varied skills in both clinical and technical aspects (settings, product characteristics, complex cases, electrophysiological measurements) and sales & business (Head of Sales, product promotion, customer relations, B2B, B2C, external and internal training sessions).

With this expertise in the field of implantable medical devices (type III) as well as in the autonomous management of several audiology practices, I wish to offer my technical, clinical, and relational skills to professionals in the sector.

Having had the opportunity to manage and successfully complete the construction of a scientific study at the National Acoustic Laboratories in Sydney, leading to its publication in a prestigious journal (Scientific Reports by Nature), I have mastered scientific terminology and the construction of clinical studies.

All these skills enable me to work in the healthcare sector and particularly with the various stakeholders involved in the medical device market.
  • French

    Native or bilingual

  • English

    Fluent

Can work on-site
Paris (up to 50km), Marseille (up to 50km)

Experience

  • EssilorLuxottica
    Consultant – Clinical evaluation of medical devices
    HEALTH AND WELLNESS
    March 2026 - Today (3 months)
    Design of clinical study protocols aimed at supporting the development of OTC hearing technologies designed to improve speech intelligibility in complex sound environments.

    - Design of clinical study protocols in accordance with the methodological and regulatory requirements applicable to medical devices (MDR, ISO 14155, good clinical practices)
    - Definition of clinical objectives, endpoints, statistical hypotheses, and evaluation methodologies
    - Contribution to the development of study designs: feasibility, pilot studies, performance studies, usability studies, comparative studies, observational studies, and PMCF
    - Development of methodologies for evaluating speech intelligibility in complex sound environments
    - Selection and standardization of audiological, cognitive tests, and PRO/MSQOL questionnaires adapted to clinical objectives
    - Construction of patient pathways and clinical investigation procedures
    - Contribution to the writing of scientific and regulatory documents: protocols, synopses, CRFs, analysis plans, clinical reports, ethics submission documents, and technical documentation
    - Critical analysis of scientific literature and support for demonstrating clinical benefit
    - Cross-functional collaboration with R&D, clinical affairs, regulatory, marketing, and UX teams
    - Support for clinical validation strategies for innovative hearing health technologies
    Audiology Clinical Research Medical Writing Medical Devices
  • Cochlear
    Consultant - Clinical Project & Training Lead
    MEDICAL
    September 2025 - Today (9 months)
    Consulting and various activities for Cochlear EMEA clinical affairs departments (France, Benelux, Africa):

    - Training Manager
    - Project Manager
    - Strategic Consultant
    - Training Development
    - Clinical and Technical Support
    - Support and operational follow-up of clinical studies
    Training Sales Management Clinical Operations
  • Cochlear
    Interim - Clinical and Technical Manager
    MEDICAL
    December 2024 - September 2025 (9 months)
    France
    Management of the Cochlear France clinical department after restructuring and before the creation of a new clinical affairs department.

    - Management and coordination of the CI clinical and technical department:
    - Leading and supervising a team of 10 people
    - Project and innovation management
    - Performance monitoring and analysis

    - Operational strategy and field implementation:
    - Definition and management of the new department structure
    - Deployment of operational strategy
    - Optimization of processes and tools

    - Market data analysis, development, and strategic alignment

    - Training, recruitment, and onboarding

    - Relationship and support with partners (KOLs, internal stakeholders)
    Leadership Team Management Clinical Strategy B2B B2C

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Education

  • Master 1 & 2 - Sensory and Motor Neuroprosthetics
    Master Biology, Mention Biology and Health - Faculty of Pharmacy - University of Montpellier
    2018
    Major de promotion
  • State Diploma - Certified Hearing Aid Specialist
    School of Audiology J.E. Bertin - Faculty of Medicine - University of Rennes 1
    2016
    Mention "Bien"

Skill set

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