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Clinical Research Associate

1 month ago

Reading, Reading, United Kingdom Pharmiweb Full time
Job Summary

We are seeking a highly experienced Clinical Research Associate to join our team in the UK. As a CRA, you will be responsible for performing site monitoring visits, adapting and driving subject recruitment plans, and ensuring the quality and integrity of study site practices.

Key Responsibilities
  • Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements
  • Work with sites to adapt and drive subject recruitment plans
  • Administer protocol and related study training to assigned sites
  • Evaluate the quality and integrity of study site practices
  • Manage the progress of assigned studies
  • Ensure documentation is maintained in accordance with GCP and local regulatory requirements
  • Collaborate with study team members for project execution support

Requirements
  • Experience of independent on-site monitoring in the UK
  • Monitoring experience of Oncology, Cardiovascular, Respiratory, Diabetic, Immunology or Renal therapeutic areas
  • Life science degree educated or equivalent industry experience
  • Flexibility to travel to sites as required

About IQVIA
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.