Clinical Research Associate, Real World Evidence

Clinical Research Associate, Real World Evidence 2 days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Join IQVIA on Our Mission to Drive Healthcare Forward IQVIA's Real World Evidence team is seeking a Clinical Research Associate (CRA I OR CRA II) to support Phase 3b and Phase 4 studies across a diverse range of therapeutic areas. The position is UK based and offers remote working with travel to sites across the UK and Ireland. Why IQVIA? IQVIA is recognized as #1 in its category on the 2025 Fortune® World’s Most Admired Companies™ list for the FOURTH consecutive year We offer genuine career development opportunities for those who want to grow as part of the organization. The chance to work on cutting‑edge medicines at the forefront of new medicines development. Responsibilities Perform site monitoring visits (selection, initiation, monitoring and close‑out) 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 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, CRF completion and submission, and data query generation and resolution. May support start‑up phase. Ensure copies/originals (as required) of 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. Requirements Experience of independent on‑site monitoring (minimum 6 months). Successfully managed multiple clinical trial protocols across diverse investigative sites. In‑depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Life science degree educated or equivalent industry experience. Flexibility to travel to sites. Apply today and forge a career with greater purpose, make an impact, and never stop learning *Please note – this role is not eligible for UK visa sponsorship* 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. Learn more at https://jobs.iqvia.com Referrals increase your chances of interviewing at IQVIA by 2x Get notified about new Clinical Research Associate jobs in Reading, England, United Kingdom. Seniority level Entry level Employment type Contract Job function Research, Analyst, and Information Technology Industries Hospitals and Health Care #J-18808-Ljbffr