{"id":551333,"url":"https://alion.io/job/iqvia-cra-ii","title":"CRA II","company":{"id":4918,"name":"IQVIA","domain":"iqvia.com","url":"https://alion.io/company/iqvia","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":78,"open_postings":523,"ghost_share":0.008,"stale_share":0.839,"repost_share":0.019,"time_to_fill_p50_days":23,"computed_at":"2026-11-02T06:13:15Z"}},"role":"Biotech","role_family":"Biotech","seniority":"middle","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Manchester, United Kingdom"],"countries":["GB"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":45000,"max_usd":109000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":533},"experience_years_min":2,"visa_sponsorship":true,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false},{"name":"Good Clinical Practice","optional":false}],"status":"live","first_seen_at":"2026-09-08T15:37:10Z","employer_posted_date":"2026-10-30","last_verified_at":"2026-11-03T02:00:55Z","board_verified":true,"closed_at":null,"days_open":55,"trust":{"level":"ok","repost_count":1,"flags":[],"days_open":54},"description":"Join IQVIA on our mission to accelerate innovation for a healthier world!\nIQVIA’s Site Management (full service / multi-sponsor) team is growing and seeking experienced Clinical Research Associates.\nWhy IQVIA?\nGenuine career development opportunities to grow as we grow\nAI-powered career advancement through our internal talent marketplace, Career Connections\nMentorship opportunities across the organisation via Employee Resource Groups\nFlexible working to assist work-life balance and professional success\nWell-being support covering your physical, mental, and financial health\nAwards\n2026 \"Glassdoor Best Place to Work in the UK\"\n#1 in category - 2026 Fortune® World’s Most Admired Companies™ list (for the FIFTH consecutive year!)\nBrandon Hall Excellence Award for Learning & Development\nResponsibilities\nPerform 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\nWork with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability\nAdminister protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues\nEvaluate 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\nManage 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\nEnsure 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\nCreate 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\nCollaborate and liaise with study team members for project execution support as appropriate\nRequirements\nRequires at least 2 years on-site monitoring experience of interventional studies\nDegree in scientific discipline or health care or equivalent industry experience\nGood knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines\nAbility to establish and maintain effective working relationships with coworkers and clients\nPlease note - this position is not eligible for visa sponsorship\nApply today and forge a career with greater purpose, make an impact, and never stop learning!\nIQVIA 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\nIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. 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