Senior / Clinical Research Associate

IQVIA

Multiple Locations
Perform site monitoring visits
Evaluate study site practices
Manage study progress tracking
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

  • Perform site monitoring visits
  • Evaluate study site practices
  • Manage study progress tracking
  • Ensure TMF and ISF maintenance
  • Create study documentation

Nice-to-have

  • Adapt subject recruitment plan
  • Collaborate with study team members
  • Effective time and financial management

Key Requirements

  • Bachelor's Degree in scientific discipline or health care
  • At least 1 year of on-site monitoring experience
  • Good Clinical Practice (GCP) and ICH guidelines knowledge
  • Proficiency in Microsoft Word, Excel and PowerPoint

Work Rights

Not specified

Tailored Resume

Cover Letter