Clinical Research Nurse - Campinas - Part Time Fix Term

IQVIA UK

Campinas, São Paulo, Brazil
Support study sites
Ensure compliance with protocols
Participant safety and advocacy
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 compliance with protocols
  • Participant safety and advocacy
  • Perform clinical procedures
  • Administer and manage study drug
  • Collect and report clinical data

Nice-to-have

  • Excellent interpersonal skills
  • High attention to detail
  • Work collaboratively with teams
  • Troubleshoot study-related issues

Key Requirements

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

Work Rights

Not specified

Tailored Resume

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