{"id":3346288,"url":"https://alion.io/job/icon-drug-safety-associate","title":"Drug Safety Associate","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":"B","score":81,"open_postings":49,"ghost_share":0,"stale_share":0.98,"repost_share":0,"time_to_fill_p50_days":12,"computed_at":"2026-10-29T05:49:05Z"}},"role":"Biotech","role_family":"Biotech","seniority":"junior","employment_type":"full_time","work_mode":"hybrid","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Tokyo, Japan","Osaka, Japan"],"countries":["JP"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":25000,"max_usd":64000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":183},"experience_years_min":1,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"live","first_seen_at":"2026-08-19T00:00:00Z","employer_posted_date":"2026-08-19","last_verified_at":"2026-10-29T17:35:48Z","board_verified":true,"closed_at":null,"days_open":71,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":71},"description":"Drug Safety Associate - Tokyo Osaka - Office HybridICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.\nAs a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.\nAs a Drug Safety Associate at ICON, you will ensure the safety of investigational drugs and contribute to the advancement of innovative treatments and therapies.\nWhat You Will Do:\nYour role will involve delivering pharmacovigilance and drug safety work to a high standard, working closely with your team and stakeholders.\nKey responsibilities include:\nCollect and review adverse event reports from clinical trials and post-marketing sources.\nConduct initial assessment and coding of adverse events according to established procedures and regulatory guidelines.\nPrepare and submit expedited safety reports to regulatory authorities and investigators as required.\nAssist in the development and maintenance of safety databases and tracking systems.\nCollaborate with cross-functional teams to ensure timely and accurate reporting of safety data.\nYour Profile:\nYou will bring relevant pharmacovigilance and drug safety experience, along with the following qualifications and skills.\nRequired qualifications and experience:\nBachelor's degree in a scientific or healthcare-related field.\n1-2 years of experience in pharmacovigilance or drug safety within the pharmaceutical or biotechnology industry preferred.\nKnowledge of pharmacovigilance regulations and guidelines (e.g., ICH, FDA, EMA).\nStrong attention to detail and ability to work effectively in a fast-paced environment.\nExcellent communication and organizational skills, with the ability to collaborate across teams and prioritize tasks efficiently.\nWillingness to travel as required (approximately 10%)\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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