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Preclinical Manager – F/H

Type de contrat : CDI
Région : Île-de-France
Niveau de formation : > Bac + 5
Rémunération : entre 50K€ et 60K€
Famille de métier : Etudes cliniques

Présentation société

cabinet de recrutement spécialisé dans le domaine du Life Sciences, du Medical Device, du Diagnostic In Vitro et des Biotechnologies.

Our client is a start-up based in Paris, named French Tech 120. A potential world-class technological leader, the company develops new innovative polymers for tissue reconstruction.

The company is looking to recruit a Preclinical Studies Manager will be a key element in the execution of the pre-clinical strategy, ensuring the collect pre-clinical data with the required quality and at the right quality to support program strategy and regulatory submissions.

The Preclinical Studies Manager will report to the Head of Preclinical. The position is based in Paris, France.

Responsibilities

  • Coordinate regulatory preclinical development studies, focused on the assessment of medical devices safety and performance in relevant animal models
  • Ensure that study design and strategy meets program requirements through close interaction with different departments (e.g. New Concepts, Product Development, Quality, Regulatory, etc)
  • Manage all preclinical operational aspects for assigned programs to ensure timely delivery of key data to inform project decisions and program milestones (availability of test items, contracts, budget, timelines, protocol development, study monitoring, data review, reporting, and study closure)
  • Oversee the progress of the study, ensuring that the study is conducted, recorded, and reported according to the study protocol and ensures that the study is compliant with the appropriate regulations
  • Managing the selection and outsourcing of studies to CROs
  • Participate in internal and supplier audits

Descriptif du profil

  • MS degree in engineering or sciences;
  • 3+ years experience in Pre-clinical studies for regulatory submissions, preferably within the medical device industry
  • Good understanding of various standards and associated requirements including ISO 13485, ISO 14971, ISO 10993, and Good Laboratory Practices (GLP)
  • Experience selecting and managing CRO relationships
  • Project management experience
  • Good team skills and ability to work in an interdisciplinary and international environment
  • Excellent oral and written communication skills (English & French)Excellent leadership skills;
  • Great communication and presentation skills;
  • Autonomy and ‘Can do’ attitude;
  • Hands-on approach;
  • Good organizational skills
  • Strong proactivity and problem-solving capabilities

Postuler

christine Horvais
contact@axemerh.com



Dernière mise à jour : 26/07/2022