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IRISOLARIS

Technicien de monitoring (H/F)

Summary: Join IRISOLARIS as a Monitoring Technician in Rousset, France, overseeing clinical trial compliance and data integrity. You'll train study staff, manage documentation, and handle adverse events. This permanent position offers a competitive salary based on experience, allowing you to contribute to vital research in a supportive environment.
IRISOLARIS
IRISOLARIS
Rousset, France   On-site   Full Time  UTC+01:00   251-500   27 days ago

IRISOLARIS

Company Overview

IRISOLARIS

Rousset, Provence-Alpes-Côte d’Azur, France

2010

Business Model

Renewable Energy

Development and manufacturing of solar energy solutions

Sales of solar panels, energy storage systems, and related services

Locations & Geography

France, Spain, Italy, Germany, and the United States

Company Culture

Their mission is to provide sustainable energy solutions that contribute to a cleaner environment.

They promote a collaborative and innovative work environment focused on employee well-being.

They offer training programs and workshops to enhance employee skills and career growth.

Activities & Projects

They are currently working on a large-scale solar farm project in southern France.

They have developed a new line of high-efficiency solar panels that increase energy output.

They implement eco-friendly practices in their manufacturing processes and supply chain.

Career Opportunities

Typical job openings include solar energy engineers, project managers, and sales representatives.

They offer competitive salaries, health benefits, and opportunities for professional development.

Contact Information

LinkedIn

Careers at IRISOLARIS


Last updated on 2025-01-31 | Report an issue

Description de poste

Missions

  • Assurer le suivi des essais cliniques en tant que Technicien de Monitoring
  • Assurer la conformité des essais cliniques avec les exigences réglementaires et les procédures internes
  • Assurer la qualité des données collectées et leur intégrité
  • Assurer la formation des investigateurs et du personnel de l'étude
  • Assurer la gestion des documents d'étude (essais cliniques, protocoles, CRF, etc.)
  • Assurer la gestion des événements indésirables et des non-conformités
  • Assurer la communication avec les investigateurs et les équipes internes
  • Participer à la rédaction des rapports d'études et des documents de soumission

Profil

  • Diplôme en sciences de la vie ou domaine connexe
  • Expérience en monitoring d'essais cliniques (minimum 2 ans)
  • Connaissance des réglementations en matière d'essais cliniques (ICH-GCP, FDA, etc.)
  • Excellentes compétences en communication écrite et verbale
  • Capacité à travailler de manière autonome et en équipe
  • Maîtrise de l'anglais (écrit et oral) est un plus

Conditions

  • CDI
  • Rousset
  • Salaire à définir selon expérience

Si vous êtes intéressé(e) par ce poste, merci d'envoyer votre CV à l'adresse suivante : [email protected]

About the role

January 12, 2025

Full Time

Company

IRISOLARIS

July 11, 2025

On-site

  •  Rousset, France

UTC+01:00

Apply now

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