(senior) Clinical Research Associate (cra)

IQVIA

Taipei, Taiwan
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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.

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 (TMF)
  • Investigator's Site File (ISF)

Nice-to-have

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

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

Work Rights

Not specified

Tailored Resume

Cover Letter