{"id":3795671,"url":"https://alion.io/job/icon-senior-pharmacovigilance-associate-3","title":"Senior Pharmacovigilance 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":"A","score":86,"open_postings":64,"ghost_share":0,"stale_share":0.75,"repost_share":0,"time_to_fill_p50_days":20,"computed_at":"2026-11-12T10:38:37Z"}},"role":"Biotech","role_family":"Biotech","seniority":"senior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Shanghai, China","Hangzhou, China"],"countries":["CN"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-11-05T09:21:39Z","employer_posted_date":"2026-11-05","last_verified_at":"2026-11-12T16:59:00Z","board_verified":true,"closed_at":null,"days_open":7,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":7},"description":"Senior Pharmacovigilance AssociateAt 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 Pharmacovigilance Associate at ICON, you will be instrumental in ensuring the safety and efficacy of pharmaceutical products by managing and oversee pharmacovigilance activities.\nWhat You Will Do:\nYou will take ownership of pharmacovigilance and drug safety deliverables, applying your expertise to complex challenges.\nKey responsibilities include:\nLeading the collection, evaluation, and processing of adverse event reports to ensure timely and accurate reporting in accordance with regulatory guidelines and company policies.\nConducting thorough data analysis and interpretation of safety data, identifying trends and potential safety signals that require further investigation.\nPreparing and submitting comprehensive periodic safety update reports (PSURs) and other regulatory documents, ensuring compliance with international regulations.\nCollaborating with medical and clinical teams to assess the clinical relevance of reported adverse events and contribute to risk management activities.\nOverseeing the maintenance and integrity of pharmacovigilance databases, ensuring accurate documentation and compliance with data management standards.\nProviding training and mentorship to junior team members on pharmacovigilance processes, regulatory requirements, and best practices.\nEngaging in audits and inspections conducted by regulatory authorities, ensuring readiness and compliance with all relevant pharmacovigilance requirements.\nYour Profile:\nYou will have a strong foundation in pharmacovigilance and drug safety, with the experience to work independently and guide others.\nRequired qualifications and experience:\nBachelor's degree in a relevant scientific discipline or healthcare-related field\nExtensive experience in pharmacovigilance or drug safety, with a strong understanding of relevant regulations and industry standards.\nProven ability to manage the pharmacovigilance process effectively, including adverse event reporting and signal detection.\nStrong analytical and critical thinking skills, with the ability to interpret complex data and make informed recommendations.\nExcellent communication and interpersonal skills, with the ability to work collaboratively across cross-functional teams.\nProficiency in pharmacovigilance databases and data management systems, as well as Microsoft Office Suite.\nAbility to work independently and manage multiple priorities in a fast-paced environment.\nWillingness to travel as required (approximately 15%)\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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