Cra 2 - Brazil

IQVIA

São Paulo, Brazil
Site monitoring visits
Gcp and ich guidelines
Subject recruitment plan
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements

Job Summary

  • Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
  • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
  • Be part of an innovative and forward-thinking company that collaborates to make a healthier world.

Matching Summary

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Skills & Requirements

Must-have

  • site monitoring visits
  • GCP and ICH guidelines
  • subject recruitment plan
  • protocol and study training
  • quality and integrity evaluation
  • Trial Master File (TMF)

Nice-to-have

  • excellent communication skills
  • problem-solving abilities
  • organizational skills
  • effective time management
  • establish working relationships

Key Requirements

  • Bachelor's Degree in scientific discipline or health care preferred
  • Excellent command of English
  • Basic knowledge of regulatory requirements
  • Good therapeutic and protocol knowledge

Work Rights

Not specified

Tailored Resume

Cover Letter