{"id":418563,"url":"https://alion.io/job/iqvia-clinical-research-associate-multi-sponsored-model","title":"Clinical Research Associate - Multi-Sponsored Model","company":{"id":4918,"name":"IQVIA","domain":"iqvia.com","url":"https://alion.io/company/iqvia","size_band":"5000+","is_staffing_agency":false,"is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":83,"open_postings":441,"ghost_share":0.002,"stale_share":0.873,"repost_share":0.016,"time_to_fill_p50_days":17,"computed_at":"2026-09-24T05:45:00Z"}},"role":"Science & Research","role_family":"Science & Research","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":["Belgrade, Serbia"],"countries":["RS"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":26000,"max_usd":65000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":219},"experience_years_min":1,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"live","first_seen_at":"2026-08-27T00:00:00Z","employer_posted_date":"2026-09-23","last_verified_at":"2026-09-24T20:18:12Z","board_verified":true,"closed_at":null,"days_open":28,"trust":{"level":"ok","repost_count":1,"flags":[],"days_open":28},"description":"If you are looking to upgrade your CRA career, this is your chance to connect with us and explore opportunities within a leading global CRO!\nWhile projects vary, your typical CRA responsibilities will include\nPerforming site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation\nSupporting the development of a subject recruitment plan\nEstablishing regular lines of communication plus administering protocol and related study training to assigned sites\nEvaluating the quality and integrity of site practices - escalating quality issues as appropriate\nManaging progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution \nYou should have\nA Bachelor's degree in a health care, MD or Pharmacist preferred.\nAt least 1 year of on-site monitoring experience.\nGood written and verbal communication skills including fluent command of English and Serbian language.\nA valid driver´s license as the role requires frequent travel to sites.\nYou will need to be comfortable collaborating and communicating with a variety of colleagues and customers. You also have a good knowledge of applicable clinical research regulatory requirements.\nApply now and let´s connect for current and/or future opportunities!\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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