Sr Cra 1

IQVIA UK

São Paulo, Brazil
On-site
Site monitoring visits
Subject recruitment plan
Protocol and regulatory adherence
IQVIA UK is seeking a Senior CRA to perform site monitoring and management for clinical studies in São Paulo, Brazil. The ideal candidate should have at least four years of on-site monitoring experience, preferably in oncology, and possess strong communication and organizational skills

Job Summary

  • Perform site monitoring visits including selection, initiation, monitoring, and close-out visits in accordance with contracted scope of work and Good Clinical Practice.
  • Manage the progress of assigned studies by tracking regulatory submissions, recruitment, CRF completion, and data query resolution.
  • Ensure the quality and integrity of study site practices and maintain documentation regarding site management and monitoring visit findings.

Matching Summary

Match Score: 85

IQVIA UK is seeking a Senior CRA to perform site monitoring and management for clinical studies in São Paulo, Brazil. The ideal candidate should have at least four years of on-site monitoring experience, preferably in oncology, and possess strong communication and organizational skills.

Skills & Requirements

Must-have

  • site monitoring visits
  • subject recruitment plan
  • protocol and regulatory adherence
  • trial master file (TMF)
  • investigator's site file (ISF)

Nice-to-have

  • effective time management
  • problem-solving skills
  • establish effective relationships

Key Requirements

  • Bachelor's Degree in scientific discipline or health care preferred
  • At least 4 years of on-site monitoring experience
  • Good knowledge of clinical research regulatory requirements (GCP, ICH)
  • Proficiency in Microsoft Word, Excel, and PowerPoint
  • Written and verbal communication skills in English

Work Rights

Not specified

Tailored Resume

Cover Letter