Cra2 - Multi-sponsor Department

IQVIA Inc

Multiple Locations
On-site
Perform site monitoring visits
Evaluate study site quality and integrity
Manage study progress and documentation
IQVIA Inc is seeking both junior and experienced Clinical Research Associates for its growing Site Management team. The role involves site monitoring visits and ensuring compliance with regulatory requirements, with a focus on managing multiple clinical trial protocols

Job Summary

  • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
  • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.

Matching Summary

Match Score: 85

IQVIA Inc is seeking both junior and experienced Clinical Research Associates for its growing Site Management team. The role involves site monitoring visits and ensuring compliance with regulatory requirements, with a focus on managing multiple clinical trial protocols.

Skills & Requirements

Must-have

  • Perform site monitoring visits
  • Evaluate study site quality and integrity
  • Manage study progress and documentation
  • Collaborate with study team members

Nice-to-have

  • Forge a career with greater purpose
  • Make an impact and never stop learning

Key Requirements

  • Experience of independent on-site monitoring
  • Managed multiple clinical trial protocols
  • In depth knowledge of GCP and ICH guidelines
  • Life science degree or equivalent industry experience
  • Flexibility to travel to sites

Work Rights

Not specified

Tailored Resume

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