Quality & Compliance Lead – Clinical Trials (Hybrid)

IQVIA LLC in Reading, Berkshire, is seeking a Sr Quality Specialist to implement the Global Quality Management Plan. You will execute quality management activities, conduct risk assessments, and support compliance with GCP and SOPs.

The ideal candidate should have a Bachelor's degree and a minimum of 4 years of clinical research experience, including monitoring experience. This role offers a hybrid working model with expected office presence of 2-3 days per week and may require occasional travel.