Experienced Clinical Research Associate Sponsor-dedicated

IQVIA

Riyadh, Saudi Arabia
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.
  • 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 study training
  • quality and integrity evaluation
  • Trial Master File maintenance
  • site documentation management

Nice-to-have

  • effective time management
  • problem-solving skills
  • client relationship building

Key Requirements

  • at least 2 years on-site monitoring experience
  • Good Clinical Practice knowledge
  • ICH guidelines knowledge
  • Arabic and English language proficiency

Work Rights

Not specified

Tailored Resume

Cover Letter