Cra2 - Argentina

IQVIA UK

Buenos Aires, Argentina
Site selection, initiation, monitoring, close-out
Protocol and related study training
Tracking regulatory submissions
You’ll have training and development to plan and progress your career in the direction you choose

Job Summary

  • You’ll have training and development to plan and progress your career in the direction you choose.
  • Award winning and innovative, we’ll give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit.
  • We are working to make a real difference in patient health, we ask you to apply now and join our team.

Matching Summary

You’ll have training and development to plan and progress your career in the direction you choose.

Skills & Requirements

Must-have

  • site selection, initiation, monitoring, close-out
  • protocol and related study training
  • tracking regulatory submissions
  • case report form completion
  • data query resolution
  • applicable clinical research regulatory requirements

Nice-to-have

  • collaborating and communicating with colleagues
  • making an impact in global research
  • improving patient outcomes and population health

Key Requirements

  • At least 2 years of on-site monitoring experience
  • Advanced in English
  • Availability to travel (50% of time)
  • Located in Buenos Aires, Argentina

Work Rights

Not specified

Tailored Resume

Cover Letter