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Clinical Research Associate

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Marseille, Provence-Alpes-Côte d'Azur, France Pharmiweb Temps plein
Job Summary

We are seeking a highly skilled Clinical Research Associate to join our team at ICON plc. As a Clinical Research Associate, you will be responsible for ensuring the smooth conduct of clinical trials, from site initiation to close-out. Your primary focus will be on ensuring compliance with regulatory requirements, managing site relationships, and maintaining accurate records.

Key Responsibilities
  • Conduct site initiation visits and ensure sites are prepared for trial start-up
  • Manage site relationships and resolve any issues that may arise during the trial
  • Ensure compliance with regulatory requirements, including GCP and ICH guidelines
  • Maintain accurate records and reports, including site visit reports and trial metrics
  • Collaborate with cross-functional teams to ensure trial success
Requirements
  • Strong experience in clinical research, preferably in a regulatory affairs or clinical operations role
  • Excellent communication and interpersonal skills
  • Ability to work independently and as part of a team
  • Strong attention to detail and organizational skills
  • Fluency in English and proficiency in French
What We Offer

At ICON, we offer a competitive salary and benefits package, as well as opportunities for professional growth and development. Our team is passionate about delivering high-quality results and making a difference in the lives of patients. If you are a motivated and detail-oriented individual with a passion for clinical research, we encourage you to apply for this exciting opportunity.