Experienced Clinical Research Associate

IQVIA

South West England, United Kingdom
Not specified (assumed hybrid or onsite based on the nature of the role)
Independent on-site monitoring experience
Good clinical practice (gcp) knowledge
Ich guidelines expertise
IQVIA is seeking experienced Clinical Research Associates in South West England to enhance their sponsor-dedicated team. The role involves performing various site monitoring activities in adherence to regulatory guidelines and supporting study execution while fostering a collaborative and innovative work environment

Job Summary

  • The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with GCP and ICH guidelines.
  • Candidates will work with sites to drive subject recruitment plans and manage study progress by tracking regulatory submissions and data queries.
  • IQVIA is recognized as a top employer with awards for being a Best Place to Work and the World's Most Admired Company.

Matching Summary

Match Score: 85

IQVIA is seeking experienced Clinical Research Associates in South West England to enhance their sponsor-dedicated team. The role involves performing various site monitoring activities in adherence to regulatory guidelines and supporting study execution while fostering a collaborative and innovative work environment.

Skills & Requirements

Must-have

  • Independent on-site monitoring experience
  • Good Clinical Practice (GCP) knowledge
  • ICH guidelines expertise

Nice-to-have

  • Flexible to travel to sites
  • Agile career opportunities
  • Collaborative team environment

Key Requirements

  • Life science degree or equivalent industry experience
  • UK work authorization required
  • No visa sponsorship available

Work Rights

Must have UK work authorization

Tailored Resume

Cover Letter