Clinical Research Associate I

3 settimane fa


Milano, Lombardia, Italia Allucent A tempo pieno

Role Overview

We are seeking a highly skilled Clinical Research Associate I to join our team at Allucent. As a key member of our clinical operations team, you will be responsible for monitoring and managing clinical trials to ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.

Key Responsibilities

  • Govern quality standards for trial monitoring activities
  • Perform selection, initiation, monitoring, and closure visits at investigator sites according to project schedules
  • Adhere to project guidelines and Allucent SOPs for monitoring requirements
  • Monitor activities at clinical study sites to ensure adherence to GCP, ICH, SOPs, and study protocols
  • Track and supervise collection of ongoing study data for regular project status reporting
  • Collect and review regulatory documents as required
  • Prepare site visit reports and telephone contact reports
  • Maintain and update CTMS in compliance with SOPs and study-specific directives
  • Act as document owner for collected documents

Requirements

  • At least 2 years of experience in clinical research
  • Strong therapeutic background
  • Ability to travel for up to 8 days on site per month, depending on project needs
  • Excellent communication and organizational skills
  • Ability to work independently and as part of a team

Benefits

  • Comprehensive benefits package
  • Competitive salary
  • Flexible working hours
  • Opportunity for remote/hybrid working
  • Leadership and mentoring opportunities
  • Access to online training and development resources


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