Clinical Research Associate, Iqvia Biotech

IQVIA Biotech

São Paulo, Brazil
On-site monitoring experience
Gcp and ich guidelines
Site selection and initiation
Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines

Job Summary

  • Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.
  • Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals.
  • Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity.

Matching Summary

Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.

Skills & Requirements

Must-have

  • on-site monitoring experience
  • GCP and ICH guidelines
  • site selection and initiation
  • subject recruitment strategies
  • essential document collection

Nice-to-have

  • agile, therapeutically aligned solutions
  • trusted partnerships
  • breakthrough treatments to patients faster
  • cross-functional project teams

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter