{"id":3346285,"url":"https://alion.io/job/icon-supervisor-pharmacovigilance-safety-reporting","title":"Supervisor, Pharmacovigilance (Safety reporting)","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":"2026-10-30T05:48:23Z"}},"role":"Biotech","role_family":"Biotech","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":["Sofia, Bulgaria","Warsaw, Poland"],"countries":["BG","PL"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":30000,"max_usd":77000,"period":"year","method":null,"sample_n":1456},"experience_years_min":null,"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":"2026-10-30T05:43:18Z","board_verified":true,"closed_at":null,"days_open":72,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":72},"description":"Supervisor Pharmacovigilance - Poland or BulgariaICON 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.\nWe are currently seeking a Supervisor, Pharmacovigilance to join our diverse and dynamic team. Within this position you will play a pivotal role in overseeing the safety monitoring and reporting of adverse events related to clinical trials and marketed products. You will contribute to ensuring patient safety and regulatory compliance through effective management of pharmacovigilance activities, coordination with cross-functional teams, and maintaining the highest standards of safety reporting.\nWhat You Will Be Doing:\nSupervising the day-to-day pharmacovigilance safety reporting operations, ensuring timely and accurate reporting to regulatory authorities.\n\nCollaborating with cross-functional teams, including clinical operations and regulatory affairs, to optimize pharmacovigilance processes.\n\nEnsuring compliance with global regulatory requirements and internal standard operating procedures for safety reporting.\n\nManaging safety submissions workflow and submission to regulatory authorities.\n\nProviding leadership and training to the pharmacovigilance team, ensuring adherence to best practices in safety reporting.\n\nYour Profile:\n8+ years in pharmacovigilance or drug safety\n\nBachelor’s degree in life sciences, pharmacy, or a related field.\n\nTeam Management skills\n\nSolid experience in pharmacovigilance or drug safety, with a focus on clinical trials or post-marketing surveillance.\n\nStrong knowledge of global pharmacovigilance regulations and guidelines.\n\nExcellent communication, leadership, and organizational skills, with the ability to manage a team effectively.\n\nDetail-oriented with the ability to manage multiple tasks and ensure accuracy in safety reporting.\n\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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