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Independent on-site monitoring experience
Knowledge of gcp and ich guidelines
Experience managing multiple clinical trial protocols
IQVIA is seeking experienced Clinical Research Associates to join their team in the UK, focusing on site monitoring and management for clinical trials. The ideal candidates will possess a strong understanding of Good Clinical Practice (GCP) and have experience in managing diverse trial protocols

Job Summary

  • Join IQVIA and contribute to driving healthcare forward.
  • Work on cutting-edge medicines and enjoy career development opportunities.
  • Collaborate with sites to enhance study performance and efficiency.

Matching Summary

Match Score: 85

IQVIA is seeking experienced Clinical Research Associates to join their team in the UK, focusing on site monitoring and management for clinical trials. The ideal candidates will possess a strong understanding of Good Clinical Practice (GCP) and have experience in managing diverse trial protocols.

Skills & Requirements

Must-have

  • Independent on-site monitoring experience
  • Knowledge of GCP and ICH guidelines
  • Experience managing multiple clinical trial protocols

Nice-to-have

  • Flexibility to travel to sites
  • Strong communication skills
  • Ability to adapt and drive recruitment plans

Key Requirements

  • Minimum 6 months of monitoring experience
  • Life science degree or equivalent experience

Work Rights

Not specified

Tailored Resume

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