{"id":3558692,"url":"https://alion.io/job/iqvia-srcra1-fsp-argentina","title":"SrCRA1 - FSP | Argentina","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":79,"open_postings":532,"ghost_share":0.008,"stale_share":0.829,"repost_share":0.019,"time_to_fill_p50_days":23,"computed_at":"2026-11-03T05:54:40Z"}},"role":"HR","role_family":"HR","seniority":"middle","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"explicit","locations":["Buenos Aires, Argentina"],"countries":["AR"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":33000,"max_usd":76000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":2146},"experience_years_min":4,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false}],"status":"live","first_seen_at":"2026-10-30T00:00:00Z","employer_posted_date":"2026-10-30","last_verified_at":"2026-11-03T07:08:29Z","board_verified":true,"closed_at":null,"days_open":4,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":4},"description":"The Senior Clinical Research Associate (CRA) will play a crucial role in the planning, execution, and management of clinical trials. This position requires a highly skilled and experienced professional who can ensure the integrity of clinical data, compliance with regulatory requirements, and the overall success of clinical research projects.\nWhile projects vary, your typical responsibilities might 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 will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.\nREQUIREMENTS\nYou should have:\nA Bachelor's degree in a health care or other scientific discipline or educational equivalent\nAt least 4 years of on-site monitoring experience.\nAdvanced in English.\nIn-depth knowledge of GCP, ICH guidelines, and regulatory requirements.\nStrong organizational and time management skills.\nExcellent communication and interpersonal skills.\nAbility to work independently and as part of a team.\nProficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.\nWillingness to travel as required.\nIf you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team.\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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