Léa Chauvigné, PhD

Clinical and Regulatory Affairs Specialist

Léa Chauvigné joined the Wyss Center in June 2022 as a Clinical Research Associate, then continued as Clinical and Regulatory Affairs Specialist in February 2024. Her role is to monitor and coordinate clinical research projects on novel medical devices to ensure compliance with protocol and regulatory standards. She is responsible for maintaining related documentation and communicating with health authorities.

Léa was previously a post-doc in the neurorehabilitation unit of the Geneva University Hospital, coordinating several clinical studies on neurological patients. She holds a Ph.D in Psychology, Neurosciences and Behavior from McMaster University (Canada) and a Masters degree in interdisciplinary neuroscience from the University of Geneva, during which she gained experience in brain imaging during interpersonal interactions.

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Contributing to

Ensuring the critical steps to reach the patient are integrated effectively
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Expertise
Decoding imagined speech from the brain
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Advance
Learning how to change your own brain activity to reduce tinnitus
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Advance
Tailoring technologies for continued recovery from chronic stroke
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Advance
Long-term brain monitoring and therapeutics for personalized management of neuro-disorders
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Team

Mar Gonzalez Fernandez

Mar Gonzalez Fernandez, MsC

Project Quality Assurance Engineer
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Celina Abi Khalil, PhD

Regulatory & Clinical Affairs Manager
Valentin

Valentin Beslouin, MSc

Quality Assurance Manager
Andreea

Andreea Mavrodin, MSc

Software Test & Quality Engineer
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Christophe Vigny

Quality Assurance Engineer