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Senior Clinical Research Specialist – F/H

Type de contrat : CDI
Région : Auvergne-Rhône-Alpes
Rémunération : non précisé
Famille de métier : Recherche clinique

Présentation société

Acteur majeur dans le domaine de la chirurgie orthopédique, Arthrex produit et distribue des dispositifs médicaux dans plus de cent pays à travers le monde. Poursuivant la mission d’aider les chirurgiens à mieux soigner leurs patients, la société Arthrex est devenue pionnière dans le domaine de l’arthroscopie et a développé plus de 18 000 produits et procédures chirurgicales offrant de réelles avancées dans la pratique de la chirurgie orthopédique mini-invasive.

o support our department Orthopedic Research in Munich or Lyon, we are currently offering a position as :


Senior Clinical Research Specialist F/M/D


Your Tasks


  • You coordinate clinical medical device studies in the EMEA region. Your focus are French-speaking countries
  • You act as the link to sites and global project members from other departments
  • You ensure compliance with national requirements in France (e.g. CNOM / ARS submissions)
  • You grow and maintain the collaboration network in French-speaking countries
  • You carry out literature and data research on current topics in the fields of orthopedics and sports medicine
  • You work closely with the regulatory department to address clinical questions
  • You develop and enhance operating procedures in accordance with relevant clinical research standards
  • You operate in your function at the Munich and Lyon offices (the primary workplace can be either of these two locations)

What You Can Expect


  • A role in an international working environment
  • Personal and appreciative collaboration
  • A future-proof position
  • Flexible working hours and the option of mobile working in many areas
  • Tailored initial training as well as comprehensive introductory training
  • Company pension and free supplementary hospital insurance
  • Free lunch from Monday to Thursday

Descriptif du profil

  • You hold a degree in Natural Sciences/a comparable field or have a equivalent qualification
  • You equally enjoy regulatory and scientific work
  • You have prior experience in clinical project management or in a coordinating function in the medical device industry
  • You are familiar with relevant international regulations, standards, and guidelines such as the MDR, ISO 14155 or the Declaration of Helsinki as well as local requirements such as the “Code de la Santé Publique”
  • You find it easy to produce scientific texts
  • You can interpret complex technical instructions and surgical procedures
  • You appreciate working in an innovative, dynamic, and global team
  • You have strong communication skills, work independently, and act responsibly
  • You are flexible and enjoy traveling
  • Very good written and verbal skills in French and English complete your profile


Charlène Daire

Dernière mise à jour : 02/01/2023