Senior / Clinical Research Associate

IQVIA UK

Multiple Locations
On-site monitoring experience
Knowledge of gcp and ich guidelines
Effective time management skills
Perform monitoring and site management work to ensure compliance with study protocols and regulations

Job Summary

  • Perform monitoring and site management work to ensure compliance with study protocols and regulations.
  • Evaluate the quality and integrity of study site practices and escalate issues as necessary.
  • Collaborate with study team members for effective project execution and support.

Matching Summary

Perform monitoring and site management work to ensure compliance with study protocols and regulations.

Skills & Requirements

Must-have

  • On-site monitoring experience
  • Knowledge of GCP and ICH guidelines
  • Effective time management skills

Nice-to-have

  • Strong organizational skills
  • Ability to establish effective relationships
  • Problem-solving skills

Key Requirements

  • Bachelor's Degree in scientific discipline
  • At least 1 year of on-site monitoring experience
  • Good command of English language

Work Rights

Not specified

Tailored Resume

Cover Letter