Clinical Research Associate, Iqvia Biotech

IQVIA UK

São Paulo, Brazil
On-site monitoring in oncology
Gcp and ich guidelines compliance
Site selection, initiation, monitoring, close-out
We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials

Job Summary

  • We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials.
  • Your work will directly contribute to the integrity and quality of clinical research data.
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Matching Summary

We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials.

Skills & Requirements

Must-have

  • on-site monitoring in oncology
  • GCP and ICH guidelines compliance
  • site selection, initiation, monitoring, close-out
  • subject recruitment strategies
  • protocol and study-specific training

Nice-to-have

  • agile, therapeutically aligned solutions
  • trusted partnerships
  • accelerate breakthrough treatments
  • improve patient outcomes

Key Requirements

  • minimum of 1 year on-site monitoring
  • Bachelor’s degree in life sciences or health-related field
  • Ability to travel as required

Work Rights

Not specified

Tailored Resume

Cover Letter