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Job Description

Clinical Research Associate II

Reading, United Kingdom Full time R1418395

Reading, United Kingdom| United Kingdom| Remote

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Job Description

IQVIA UK are seeking Clinical Research Associates (CRA II / SR CRA) to strengthen our cFSP (sponsor dedicated) business unit.

By joining IQVIA you’ll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.

Responsibilities

  • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
  • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
  • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
  • Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
  • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
  • Collaborate and liaise with study team members for project execution support as appropriate
  • If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis

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
  • UK driving license and access to vehicle (excluding London travel zones 1 & 2) and flexibility to travel to sites as required

This role is not eligible for UK visa sponsorship

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

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