Pharmacovigilance
494 open positions
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Medical Monitor (Canada Board-Certified Psychiatrist) Psi-CroRemote 14d Provides medical input to global clinical studies, advises teams on safety, and monitors trial participant safety.
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Patient Safety Risk & Signal Management Product Lead AstraZenecaMölndal, , Sweden 14d Lead the technology strategy and product delivery for enterprise safety platforms (NGSMS, ORBIT) to support global pharmacovigilance operations, signal detection, benefit-risk evaluation, and risk management planning.
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Senior Clinical Trial Case Manager↗ CslMaidenhead, England, UK 14d Subject matter expert managing case management activities, safety reporting plans, and vendor oversight for assigned clinical trials to ensure GxP compliance.
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Practicante Farmacovigilancia↗ Eli Lilly and Company 14d Receive, compile, document, and translate adverse event reports from Spanish to English for the company's Pharmacovigilance database received at the Colombia affiliate.
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University Intern - Patient Safety & Pharmacovigilance↗ Boehringer IngelheimWinnersh, England, UK £26k14d Support the Patient Safety & Pharmacovigilance team in monitoring medicine safety, identifying risks, and ensuring compliance with regulatory requirements.
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Medical Product Safety & Risk Investigation Analyst↗ Gc Technologies Pvt LtdHyderabad, Telangana, India 14d Conduct investigations into medical product safety issues, identify suspicious activities, and recommend corrective actions to ensure compliance with FDA regulations.
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Safety Reporting Specialist ThermofisherRemote, Mexico 14d Manage and coordinate the production of regulatory and safety reports, ensure accurate documentation of adverse events, and support compliance with global pharmacovigilance requirements.
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Global Pharmacovigilance Data Management Manager BaxterRemote €45k14d Lead a global Pharmacovigilance Data Management team to manage operations, optimize processes, and ensure timely delivery of patient safety data across Europe, Asia-Pacific, and the US.
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Senior Manager, Data Management, Office of Safety Operations - Hybrid, Chicago AbbVieNorth Chicago, IL, us 15d Senior Manager driving data operations, governance, and continuous improvement to deliver high-quality, timely safety data solutions for regulatory reporting and product surveillance.
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Pharmacovigilance Specialist↗ Bausch + LombMH, IN 15d Ensure vendor case processing quality and compliance for Individual Case Safety Reports (ICSRs) and device events, while managing Post-Marketing Surveillance (PMS) and medical device safety reporting.
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Safety Data Lead I MsdCHN - Beijing - Beijing (Wangjing Park), CN 15d Analysis and interpretation of adverse event (AE) reports for investigational and marketed products in compliance with regulatory requirements.
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Senior Drug Safety Physician↗ SoteriusRemote, IN 15d Senior Drug Safety Physician performing medical review of aggregate reports, signal detection/management, and risk minimization activities.
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SERM Principal Scientist↗ GskLondon, ENG, GB 15d Provides medical/scientific knowledge in the safety evaluation and risk management of GSK products in clinical development and post-marketing settings.
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Senior Criminal Enforcement Officer, Disclosure Officer - £43,894 (National) or £47,776 (London) p.a. + benefits↗ Medicines and Healthcare Products Regulatory AgencyRemote £44k–£48k15d Leading and managing disclosure in complex criminal investigations involving medicines and medical devices, ensuring compliance with CPIA requirements and advising investigators and prosecutors.
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Pharmacovigilance Associate Harrow HealthRemote 15d Support medical information inquiries, adverse event reporting, and product quality complaints to ensure the safety and regulatory compliance of ophthalmic drug products.
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Patient Safety Intern Summer 2027 BristolmyerssquibbPrinceton - NJ - US 15d Support strategic initiatives in pharmacovigilance and drug safety by conducting research, analyzing safety data, and generating reports to inform patient safety strategies.
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Med Data Review Assoc Mgr↗ FortreaBengaluru, Karnataka, India 15d Manage Central Medical Review activities, including tool configuration, plan development, and safety signal evaluation for clinical studies.
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Patient Safety Intern Summer 2027 BmsPrinceton - NJ - US 15d Support strategic initiatives in pharmacovigilance and drug safety by conducting research, analyzing safety data, and generating operational metrics to inform patient-centric safety strategies.
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Pessoa Coordenadora de Farmacovigilância e Segurança do Paciente↗ MetarhSão Paulo, São Paulo, Brazil 15d Leading a team of 8-10 professionals to manage Pharmacovigilance/Drug Safety operations, ensuring regulatory compliance, quality, and SLA delivery.
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Pharmacovigilance Quality & Compliance Manager SanofiTokyo, JP 15d Ensure compliance with local PV regulations and global procedures for Japan PV business, including QD management, self-inspection, and document control.
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Safety & PV Specialist (SS I) - Night Shift (Gurugram) Syneos HealthIndia 15d Process and track Individual Case Safety Reports (ICSRs) for clinical trials and post-marketing programs, ensuring data accuracy and regulatory compliance.
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Chargé de Pharmacovigilance F/H IVIDATARemote 17d Manage and follow up on pharmacovigilance cases, ensuring data quality, medical review, and reporting for an international pharmaceutical client.
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Associate Marketed Project Safety Director - Sponsor Dedicated IqviaBucuresti, Romania 17d Deputy QPPV responsible for establishing and maintaining the pharmacovigilance system for marketed products in the EU/EEA, assisting the QPPV with regulatory compliance, risk evaluation, and safety data management.
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Pharmacovigilance Associate - VIE Contract Sanofi GroupSingapore 18d Assist with pharmacovigilance responsibilities ensuring corporate and regulatory requirements are met for all Sanofi products in Singapore.
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Mitarbeiter Arzneimittelsicherheit / Complaint Management (m/w/d) ROTOP Pharmaka GmbHDresden 18d Managing drug safety complaints (ICSRs), product quality complaints, and medical-pharmaceutical inquiries for a radiopharmaceutical company.
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Director, Pharmacovigilance Alliance Contracting and Management Johnson and JohnsonBeerse, Turnhout 18d Strategic leadership and executive oversight of Pharmacovigilance (PV) contractual relationships and alliance partnerships between IM OCMO and external partners.
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Manager, Global Patient Safety Scientist RegeneronWarren, US $115k–$187k18d Lead safety strategies for molecules in clinical development and post-marketing phases, including data aggregation, review, analysis, and benefit-risk assessment.
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Associate Director / Director - Regional Pharmacovigilance Leader (Asia PAC)↗ Eli LillySydney, NSW, AU 18d Provide operational and people leadership for regional pharmacovigilance activities, translating global strategy into consistent execution across the Asia Pacific region.
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Sr Mgr Regulatory Compliance - Medical Events, Vigilance & AE Case Reporting MedlineNorthfield, Illinois, US $154k–$231k18d Lead global medical device vigilance and pharmacovigilance activities, including adverse event case management, regulatory reporting, and safety signal detection for drugs, biologics, combination products, and consumer products.
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Director - Japan Safety Strategy VeevaJapan - Tokyo 19d Director responsible for growing and sustaining Veeva's Japan market share for Vault safety applications (Safety, Safety.AI, SafetyDocs, Safety Signal) and providing thought leadership and sales support.
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Medical Information Specialist - German & English speaking EversanaWarsaw, Masovian Voivodeship, pl 19d Respond to drug information inquiries from healthcare professionals and patients, identify adverse events, and perform medical writing for a pharmaceutical client.
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Safety Officer Business Intelligence ExcelyaParis, Ile-de-France 20d Pharmacovigilance Business Intelligence & Aggregate Safety Reporting Analyst ensuring continuity of a key function in an international environment by gathering user needs and translating them into compliant GxP solutions.
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Medical Project Coord↗ Thermo Fisher ScientificSão Paulo, SP, BR 20d Coordinate and review safety data, identify trends, and support drug safety operations to ensure compliance and patient safety in clinical trials.
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Patient Safety Associate I (Drug Safety Associate I)↗ ParexelRemote 20d Process individual case safety reports, conduct literature reviews, and manage regulatory submissions to ensure safe therapy development.
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