Experienced Clinical Research Associate Sponsor-dedicated

IQVIA

Dubai, United Arab Emirates
Site monitoring visits
Subject recruitment plan
Protocol and study training
Perform monitoring and site management work to ensure sites comply with study protocols, regulations, and sponsor requirements

Job Summary

  • Perform monitoring and site management work to ensure sites comply with study protocols, regulations, and sponsor requirements.
  • Manage study progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution.
  • Ensure site documents are maintained in accordance with GCP and local regulatory requirements, and create documentation for site management and monitoring findings.

Matching Summary

Perform monitoring and site management work to ensure sites comply with study protocols, regulations, and sponsor requirements.

Skills & Requirements

Must-have

  • Site monitoring visits
  • Subject recruitment plan
  • Protocol and study training
  • Quality and integrity evaluation
  • Trial Master File (TMF)
  • Investigator's Site File (ISF)

Nice-to-have

  • Effective time management
  • Problem-solving skills
  • Client relationship building

Key Requirements

  • Minimum 2 years on-site monitoring experience
  • Good Clinical Practice (GCP)
  • ICH guidelines knowledge
  • Proficiency in Microsoft Office Suite
  • Arabic and English language proficiency

Work Rights

Not specified

Tailored Resume

Cover Letter