Experienced Clinical Research Associate

IQVIA

New Cairo, Egypt
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.
  • Collaborate and liaise with study team members for project execution support as appropriate.

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
  • subject recruitment plan
  • data query resolution

Nice-to-have

  • effective time management
  • problem-solving 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) and ICH guidelines knowledge
  • Proficiency in Microsoft Word, Excel, PowerPoint
  • Fluency in Arabic, good command of English

Work Rights

Not specified

Tailored Resume

Cover Letter