{"id":3050843,"url":"https://alion.io/job/icon-clinical-trial-coordinator","title":"Clinical Trial Coordinator","company":{"id":5677,"name":"ICON","domain":"iconplc.com","url":"https://alion.io/company/icon","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":null},"role":"Administrative","role_family":"Administrative","seniority":null,"employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Santiago, Chile"],"countries":["CL"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":10000,"max_usd":21000,"period":"year","method":null,"sample_n":14242},"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false},{"name":"Good Clinical Practice","optional":false}],"status":"closed","first_seen_at":"2026-10-21T00:00:00Z","employer_posted_date":"2026-10-21","last_verified_at":"2026-10-25T07:23:38Z","board_verified":false,"closed_at":"2026-10-25T07:23:38Z","days_open":4,"trust":{"level":"not_scored","repost_count":null,"flags":[],"days_open":4},"description":"Clinical Trial Coordinator - Hybrid - Santiago, ChileAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.\nAs the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.\nAs a SMA I at ICON, you will support the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintain high standards of operational efficiency.\nWhat You Will Do:\nYour role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.\nKey responsibilities include:\nAssisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.\nSupporting site management activities, including documentation preparation, data entry, and tracking site performance metrics.\nCollaborating with cross-functional teams to facilitate communication and address site-related issues effectively.\nMaintaining accurate records of site activities and contributing to the preparation of monitoring reports.\nParticipating in training and development initiatives to enhance knowledge and skills in clinical trial management.\nYour Profile:\nYou will bring relevant clinical research experience, along with the following qualifications and skills.\nRequired qualifications and experience:\nBachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research.\nSome experience in clinical research, site management, or related administrative roles is preferred but not mandatory.\nStrong organizational skills and attention to detail, with the ability to manage multiple tasks effectively.\nBasic knowledge of clinical trial processes and regulatory requirements is a plus.\nExcellent communication and interpersonal skills, with the ability to work collaboratively within a team environment.\nWillingness to travel as required (approximately 25%)\nEmployment with ICON is contingent upon having the legal right to work in the country where the role is based.\nRewards & Benefits\nICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.\nBenefits may include:\nCompetitive base salary and performance related incentives\nHealth and wellbeing programmes including medical, dental, and vision coverage where applicable\nRetirement and pension plans\nLife assurance and disability coverage\nEmployee assistance programmes and wellbeing resources\nLearning and development opportunities through structured training and career pathways\nBenefits may vary depending on role and location.\nVisit our careers site to read more about the benefits ICON offers.\nInclusion and Accessibility\nICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.\nIf you require reasonable accommodations during the recruitment process, please let us know or submit a request here.\nAre you a current ICON Employee? 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