Clinical Research Associate, Site Management - Italy

IQVIA UK

Italy
Good clinical practice (gcp) adherence
Protocol and regulatory training completion
Site monitoring visit execution
The role involves engaging in a structured training program to independently conduct clinical monitoring visits according to study protocols and GCP

Job Summary

  • The role involves engaging in a structured training program to independently conduct clinical monitoring visits according to study protocols and GCP.
  • Candidates will be responsible for evaluating site practices, managing regulatory submissions, and ensuring the integrity of the Trial Master File.
  • This position requires close collaboration with study teams to support project execution and enhance site recruitment predictability.

Matching Summary

The role involves engaging in a structured training program to independently conduct clinical monitoring visits according to study protocols and GCP.

Skills & Requirements

Must-have

  • Good Clinical Practice (GCP) adherence
  • Protocol and regulatory training completion
  • Site monitoring visit execution
  • Trial Master File (TMF) maintenance
  • Case Report Form (CRF) management

Nice-to-have

  • Strong organizational and problem-solving skills
  • Effective time and financial management
  • Ability to establish client relationships
  • Experience with subject recruitment planning

Key Requirements

  • Bachelor's Degree in scientific discipline or healthcare
  • Local ministerial decree as per Italian requirements
  • Prior clinical experience preferred
  • Proficiency in Microsoft Office and mobile devices
  • Advanced knowledge of GCP and ICH guidelines

Work Rights

Must possess local ministerial decree as per Italian requirements

Tailored Resume

Cover Letter