Experienced Clinical Research Associate

IQVIA UK

New Cairo, Egypt
Site monitoring visits
Subject recruitment plan
Protocol and 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.
  • 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
  • subject recruitment plan
  • protocol and training
  • quality and integrity evaluation
  • study progress management
  • site document filing
  • site management documentation

Nice-to-have

  • effective time management
  • financial management skills
  • establish working relationships

Key Requirements

  • At least 1 year on-site monitoring experience
  • Bachelor's Degree in scientific discipline or health care preferred
  • Good Clinical Practice (GCP) knowledge
  • International Conference on Harmonization (ICH) guidelines knowledge
  • Proficiency in Microsoft Word, Excel and PowerPoint
  • Fluency in Arabic
  • Good command of English language

Work Rights

Not specified

Tailored Resume

Cover Letter