{"id":3335888,"url":"https://alion.io/job/iqvia-cra2","title":"CRA2","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":84,"open_postings":581,"ghost_share":0.014,"stale_share":0.783,"repost_share":0.036,"time_to_fill_p50_days":21,"computed_at":"2026-10-30T05:48:23Z"}},"role":"HR","role_family":"HR","seniority":"junior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Porto, Portugal"],"countries":["PT"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":17500,"max_usd":46000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":2951},"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"Good Clinical Practice","optional":false},{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-10-26T00:00:00Z","employer_posted_date":"2026-10-26","last_verified_at":"2026-10-30T05:44:04Z","board_verified":true,"closed_at":null,"days_open":4,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":4},"description":"Your responsibilities will include:\nPerforming site selection, initiation, monitoring and close-out visits\nSupporting the development of a subject recruitment plan\nEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines\nManaging progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions\nCollaborating with experts at study sites and with client representatives\nQualifications:\nUniversity degree in scientific discipline or health care\n2-4 years of independent on-site monitoring experience.\nVery good computer skills including MS Office\nExcellent command of Portuguese and English language.\nOrganizational, time management and problem-solving skills\nAbility to establish and maintain effective working relationships with coworkers, managers, and clients\nFlexibility to travel\nDriver’s license class B\nWhat you can expect:\nResources that promote your career growth\nLeaders that support flexible work schedules\nPrograms to help you build your therapeutic knowledge\nExcellent working environment in a stabile, international, reputable company\nCompany car, mobile phone and attractive benefits package\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. We appreciate your honesty and professionalism.\nAt IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. 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