Experienced Clinical Research Associate

IQVIA UK

Netanya, Israel
Site monitoring visits
Subject recruitment planning
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 planning
  • Protocol and study training
  • Quality and integrity evaluation
  • Study progress management
  • Trial Master File documentation

Nice-to-have

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

Key Requirements

  • At least 3 years on-site monitoring experience
  • Good Clinical Practice (GCP) knowledge
  • International Conference on Harmonization (ICH) guidelines
  • Proficiency in Microsoft Word, Excel, PowerPoint
  • High School Diploma or equivalent

Work Rights

Not specified

Tailored Resume

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