Clinical Research Associate

IQVIA

Sofia, Bulgaria
Site monitoring visits
Protocol adherence
Regulatory requirements
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.
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

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
  • protocol adherence
  • regulatory requirements
  • GCP and ICH guidelines
  • subject recruitment plan

Nice-to-have

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

Key Requirements

  • 1 year on-site monitoring experience
  • Bachelor's Degree in scientific discipline or health care preferred
  • Good knowledge of regulatory requirements
  • Computer proficiency
  • Written and verbal communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter