{"id":3265096,"url":"https://alion.io/job/icon-technical-quality-expert","title":"Technical Quality Expert","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":48,"ghost_share":0,"stale_share":0.958,"repost_share":0,"time_to_fill_p50_days":16,"computed_at":"2026-11-03T05:54:40Z"}},"role":"Sales","role_family":"Sales","seniority":"senior","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"],"countries":["JP"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":36000,"max_usd":79000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":13},"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"closed","first_seen_at":"2026-10-06T00:00:00Z","employer_posted_date":"2026-10-06","last_verified_at":"2026-10-30T19:16:20Z","board_verified":false,"closed_at":"2026-10-30T19:16:20Z","days_open":24,"trust":{"level":"not_scored","repost_count":null,"flags":[],"days_open":24},"description":"Technical Quality Expert - Tokyo Osaka - Office Hybrid RemoteAt 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 Senior Medical Editor at ICON, you will be responsible for ensuring the accuracy, clarity, and quality of scientific documents and publications related to clinical trials.\nWhat You Will Do:\nYour experience in editorial and content services will be key in delivering high-quality outcomes and mentoring colleagues.\nKey responsibilities include:\nEditing and proofreading a wide range of scientific documents, including clinical study reports, regulatory submissions, publications, and presentations, ensuring adherence to quality standards and consistency.\nCollaborating with medical writers to improve the clarity and effectiveness of scientific content, providing guidance on structure, style, and language.\nEnsuring compliance with applicable regulatory requirements, guidelines, and best practices in medical writing and publishing.\nProviding mentorship and training to junior editors and medical writers, fostering a culture of continuous improvement and excellence in scientific communication.\nConducting thorough fact-checking and verification of data to ensure accuracy and reliability of published materials.\nStaying updated with industry trends, regulatory changes, and advancements in medical writing and editing practices.\nParticipating in the development and implementation of standard operating procedures (SOPs) related to document editing and quality control.\nYour Profile:\nYou will have a strong foundation in editorial and content services, with the experience to work independently and guide others.\nRequired qualifications and experience:\nBachelor's degree in a relevant scientific discipline or communications-related field\nExtensive experience in medical editing, with a strong understanding of clinical research and regulatory documentation.\nExceptional editing and proofreading skills, with a keen eye for detail and the ability to enhance the clarity and impact of scientific content.\nStrong knowledge of medical terminology and scientific writing conventions, with experience in using editing style guides.\nExcellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and stakeholders.\nProficiency in editing software and tools, as well as document management systems.\nDemonstrated ability to manage multiple projects and meet deadlines in a fast-paced environment.\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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