{"id":4321164,"url":"https://alion.io/job/icon-sma-i-6","title":"SMA I","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":{"grade":"A","score":86,"open_postings":65,"ghost_share":0,"stale_share":0.754,"repost_share":0,"time_to_fill_p50_days":20,"computed_at":"2026-11-14T05:58:10Z"}},"role":"Sales","role_family":"Sales","seniority":null,"employment_type":"full_time","work_mode":"remote","remote_scope":"stated_countries","remote_scope_basis":"board_field","remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Beijing, China","Shanghai, China"],"countries":["CN"],"hiring_countries":["CN"],"hiring_countries_total":1,"salary":null,"salary_estimate":null,"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":"live","first_seen_at":"2026-11-13T00:00:00Z","employer_posted_date":"2026-11-13","last_verified_at":"2026-11-14T20:30:00Z","board_verified":true,"closed_at":null,"days_open":1,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":1},"description":"Site Management Associate, ChinaAt 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:\nCoordinate site study activities, visits, documents and participant workflows.\nMaintain essential records and accurate study system information.\nSupport investigators and site staff with study requirements and issue resolution.\nTrack milestones, recruitment and operational risks.\nEnsure site activities follow protocol, GCP and local procedures.\nRequired qualifications and experience\nBachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research.\nKnowledge of clinical trial conduct and ICH Good Clinical Practice (GCP).\nExperience coordinating site study activities, visits, documents and participant workflows.\nExperience maintaining essential records and accurate study system information.\nExperience supporting investigators and site staff with study requirements and issue resolution.\nExperience tracking milestones, recruitment and operational risks.\nPreferred qualifications and experience\nSome experience in clinical research, site management, or related administrative roles mandatory.\nBasic knowledge of clinical trial processes and regulatory requirements.\nClinical research coordinator or site management experience.\nCurrent ICH Good Clinical Practice (GCP) training.\nExperience with electronic data capture (EDC), clinical trial management systems (CTMS) or electronic health records.\nWorking conditions\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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Docs: https://alion.io/developers"}}