Clinical Research Associate, Site Management - Italy

IQVIA UK

Milan, Italy
Good clinical practice
Ich guidelines
Protocol requirements
Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements

Job Summary

  • Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.
  • Under close supervision, perform site monitoring visits (selection, initiation, monitoring and close out visits) in accordance with contracted scope of work and good clinical practices.
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Matching Summary

Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.

Skills & Requirements

Must-have

  • Good Clinical Practice
  • ICH guidelines
  • protocol requirements
  • site monitoring visits
  • TMF filing

Nice-to-have

  • effective time management
  • problem-solving skills
  • client relationship management

Key Requirements

  • Bachelor's Degree in scientific discipline or health care
  • Local ministerial decree requirements
  • At least 1 year prior clinical experience
  • Proficiency in Microsoft Office Suite
  • Good command of English language

Work Rights

Not specified

Tailored Resume

Cover Letter