Clinical Research Associate

7 giorni fa


Milano, Lombardia, Italia Allucent A tempo pieno
Job Summary

We are seeking a highly skilled Clinical Research Associate to join our team at Allucent. As a Clinical Research Associate, you will be responsible for monitoring and managing clinical trials at investigator sites, ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements.

Key Responsibilities:

  • Conduct site initiation, monitoring, and closure visits to ensure compliance with study protocols and regulations.
  • Review and verify data collected from investigator sites to ensure accuracy and completeness.
  • Identify and report any issues or concerns related to study conduct or site performance.
  • Collaborate with project team members to ensure timely completion of study milestones.
  • Develop and maintain strong relationships with investigator sites and site staff.

Requirements:

  • At least three years of clinical monitoring experience or relevant clinical trial experience.
  • Relevant life science degree or healthcare background.
  • Strong knowledge of medical terminology and clinical monitoring processes.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and as part of a team.

What We Offer:

  • Competitive salary and benefits package.
  • Opportunities for professional growth and development.
  • Collaborative and dynamic work environment.
  • Flexible working hours and remote work options.

About Allucent:

Allucent is a leading provider of clinical trial services, dedicated to helping small to medium-sized biopharmaceutical companies navigate the complex world of clinical trials. We are committed to delivering high-quality services and building strong relationships with our clients and partners.



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