Clinical Research Nurse - Campinas - Part Time Fix Term

IQVIA

Campinas, São Paulo, Brazil
Support study sites
Ensure participant safety
Perform clinical procedures
Support study sites in coordinating Phase I–IV clinical research studies, ensuring compliance with study protocols, SOPs, GCP, and all applicable regulations

Job Summary

  • Support study sites in coordinating Phase I–IV clinical research studies, ensuring compliance with study protocols, SOPs, GCP, and all applicable regulations.
  • Contribute to participant safety, clinical procedures, study documentation, and operational workflow under the supervision of the Principal Investigator.
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Matching Summary

Support study sites in coordinating Phase I–IV clinical research studies, ensuring compliance with study protocols, SOPs, GCP, and all applicable regulations.

Skills & Requirements

Must-have

  • Support study sites
  • Ensure participant safety
  • Perform clinical procedures
  • Administer study drug
  • Collect and report clinical data
  • Maintain protocol compliance

Nice-to-have

  • Volunteer advocate
  • Troubleshoot study-related issues
  • Collaborate with monitors
  • High attention to detail

Key Requirements

  • Nursing degree
  • Minimum 1 year relevant experience
  • Strong knowledge of clinical trials and GCP
  • Proficiency in MS Windows and Office
  • Strong English communication skills
  • Active nursing license

Work Rights

Not specified

Tailored Resume

Cover Letter