Acra

IQVIA

São Paulo, Brazil
Site monitoring visits
Subject recruitment plan
Protocol and study training
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.
  • Collaborate and liaise with study team members for project execution support as appropriate.
  • 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
  • Subject recruitment plan
  • Protocol and study training
  • Study site practices evaluation
  • Trial Master File (TMF)
  • Investigator's Site File (ISF)

Nice-to-have

  • Excellent problem-solving judgment
  • Effective time financial management
  • Adaptability and innovation

Key Requirements

  • Bachelor's Degree in scientific discipline or health care preferred
  • Excellent command of English
  • Basic knowledge of GCP and ICH guidelines
  • Proficiency in Microsoft Word, Excel and PowerPoint

Work Rights

Not specified

Tailored Resume

Cover Letter