Pharmacovigilance
495 open positions
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Manager, Pharmacovigilance IconIndia, Chennai 5d Overseeing pharmacovigilance activities to ensure the safety and efficacy of clinical trial products throughout their lifecycle.
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SERM Medical Director / SERM Scientific Director GskWarsaw, PL €419k5d Provides in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK assets for complex Classic & Established Products with ongoing litigation.
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Manager Triage RegeneronHyderabad, IN 5d First medical point of contact for Individual Case Safety Reports, assessing seriousness, expectedness, and causality to guide cases into regulatory workflows.
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Manager, Pharmacovigilance↗ ICON PlcChennai, Tamil Nadu, India 5d Overseeing pharmacovigilance activities to ensure the safety and efficacy of clinical trial products throughout their lifecycle.
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Expert:in für Arzneimittelsicherheit↗ K-Recruiting Life SciencesBaden-Württemberg, Germany 5d Lead global pharmacovigilance operations and trial management, acting as a deputy Qualified Person for Pharmacovigilance (QPPV) and Global Safety Physician.
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Spezialist Pharmakovigilanz (m/w/d)↗ Randstad DeutschlandDresden, Saxony, Germany 5d Manage adverse event reporting (ICSRs) and pharmaceutical complaints for a global pharma company, with a path to assume statutory safety officer roles.
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Medical Monitor (Oncology)↗ Psi CroOxford, ENG, GB 5d Provide medical oversight and expertise for global oncology clinical trials, ensuring participant safety and scientific quality.
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DSMB Member (Physician)↗ Sitero LLCRemote 5d Independent physician expert reviewing interim clinical trial data to ensure participant safety, data integrity, and regulatory compliance for early-phase biologic studies.
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Medical Information Specialist I - Nurse (Hybrid) ThermofisherSaint-Laurent, Canada 5d Provide technical and medical information, intake adverse events/product complaints, and research inquiries for pharmaceutical or device products.
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Associate Director, Senior Patient Safety Scientist AstraZenecaUS - Gaithersburg - MD 5d Leads the review of safety data and documents for potential safety issues, authors regulatory reports, and presents safety analyses to committees.
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Regulatory Affairs & Pharmacovigilance Manager Medison PharmaBucurești, Romania 6d Oversee regulatory and pharmacovigilance operations for the Central Cluster (Romania, Moldova, Hungary, Czech Republic, Slovakia) to ensure compliance with local and international requirements and support product lifecycle management.
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Medical Monitor↗ NovotechCarlton, Victoria, Australia 6d Provide medical oversight for clinical trials, develop monitoring plans, and review protocols and safety data for Novotech-sponsored studies.
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Director, Patient Safety (MD) GileadUnited States - New Jersey - Parsippany $221k–$286k6d Lead safety activities for CAR-T clinical development programs, shaping the safety profile of innovative cell therapies and ensuring regulatory compliance.
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Service Area Manager- Literature Surveillance↗ Productlife Group 6d Lead Literature Surveillance activities and team in India, ensuring compliant delivery of global and local surveillance across multiple clients.
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SME-Medical Safety↗ Cognizant 6d Subject matter expert in medical safety supporting safe and effective product development in pharma R&D by interpreting clinical and nonclinical data, assessing risks, and ensuring regulatory compliance.
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PHARMACOVIGILANCE AUDITOR↗ PharmalexMadrid, Community of Madrid, Spain 6d Lead and coordinate GVP audits (process, system, document) for pharmaceutical clients, acting as an external consultant for quality assurance and regulatory compliance.
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Medical Safety Expert, Sandoz↗ Sandoz IndiaTelangana, India 6d Provides support for delivery activities including co-authoring safety documents, monitoring product safety profiles, and responding to Health Authority queries.
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Product Safety Manager↗ ElancoKA, IN 6d Conduct systematic surveillance and review of scientific literature to identify, assess, and document safety information for non-High Profile Products to support benefit-risk assessments and regulatory compliance.
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Principal Medical Safety Specialist - CRMDx BostonscientificArden Hills US-MN, United States | US-MA-Marlborough, US-MN-Arden Hills $102k–$194k6d Principal Medical Safety Specialist providing medical and clinical safety expertise across the total product lifecycle for cardiology and electrophysiology products and therapies.
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PHARMACOVIGILANCE AUDITOR MyhrabcWEMEA > Spain > Madrid - Orense 6d Lead and coordinate GVP audits (process, system, document) for pharmaceutical clients, acting as an external consultant for quality assurance and improvement of pharmacovigilance systems.
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Pharmacovigilance Specialist with French↗ IqviaRemote 6d Review, assess, and process safety data and information across service lines, including collecting and tracking incoming Adverse Events (AEs), database entry, coding AEs and products, writing narratives, and literature-related activities.
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Medical Information Specialist EversanaOverland Park, KS, us 6d Provide scientifically balanced, evidence-based medical information to healthcare professionals, patients, and payers; handle adverse events and product complaints; and create medical writing responses.
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Safety & PV Submission Spec I JobgetherRemote 7d Support the preparation, coordination, and submission of critical pharmacovigilance and drug safety reports to regulatory authorities, ethics committees, and clinical investigators.
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Lead Pharmacist, Medicines Safety Officer↗ University Hospitals Coventry and Warwickshire (uhcw) Nhs TrustCoventry, England, UK 7d Lead the organization's medication incident reporting, learning, and risk management to ensure safe medicine use across the hospital.
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Drug Safety Scientist↗ Fresenius Kabi USALake Zurich, IL, US $110k–$115k7d Receives, assesses, obtains follow-up, and reports adverse drug events for company drug products, ensuring compliance with global and local regulations.
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Drug Safety Scientist FreseniusglobalLake Zurich, IL, US $110k–$115k7d Receives, assesses, obtains follow-up, and reports adverse drug events for company drug products, preparing Periodic Adverse Drug Experience Reports (PADER) and coordinating FDA submissions.
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Associate MDR/Vigilance Specialist↗ Hero RecruitmentGalway, County Galway, Ireland 7d Monitors drug and medical device surveillance programs, processes adverse event reports, and ensures compliance with regulatory requirements for Medical Device Reports (MDRs) and Adverse Drug Experience (ADE) data.
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Manager, Local Literature Surveillance↗ Johnson & Johnson Innovative MedicineLisbon, Lisbon, Portugal 7d Strategic oversight and continuous improvement of local literature surveillance activities across 80+ territories to support global pharmacovigilance obligations.
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Scientific Director (SERM & Clinical Safety & Pharmacovigilance) - Remote - Based in Brazil↗ Alphanumeric SystemsRemote 7d Provide scientific leadership in product safety evaluation, benefit-risk management, and pharmacovigilance across clinical and post-marketing programs.
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Associate Pharmacovigilance - Freshers↗ ClinoGenesis Research InstituteRemote 7d Entry-level associate responsible for processing Individual Case Safety Reports (ICSRs), data entry, and medical coding of adverse events in drug safety operations.
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Pharmacovigilance Intake Specialist BaxterWarsaw, Masovian, PL PLN 112k7d Member of the Safety Operations team handling country-level pharmacovigilance activities including collection, documentation, and processing of local adverse event (AE) reports.
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Manager, PST Program Management AbbVieNorth Chicago, IL, us 7d Shape and drive strategic priorities for the Product Safety Team (PST) to characterize drug safety profiles and maximize benefit-risk for patients worldwide.
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Virtual Info Session for Nursing Professionals MedpaceNavi Mumbai, India 8d Transition clinical nursing knowledge into office-based corporate roles reviewing clinical trial data and managing patient safety events.
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Drug Safety Associate - 6-Month Contract↗ CencoraOntario, Canada 8d Receive, scan, document, and triage adverse event information and product quality complaints for Cencora's patient and provider support and pharma commercialization services in Canada.
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Pharmacovigilance Technology Product Lead (Signal & Risk Management)↗ Discover InternationalVästra Götaland County, Sweden 8d Own the product roadmap and technology strategy for signal detection, benefit-risk, and risk management platforms supporting global pharmacovigilance operations.
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Clinical Trial Manager↗ SciproMunich, Bavaria, Germany 8d Ensure clinical trials comply with safety regulations, coordinate adverse event reporting, and review clinical data for safety concerns.
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PV Specialist - EUG Operations↗ Dr. Reddy's LaboratoriesHyderabad, Telangana, India 8d Support Pharmacovigilance activities for the European Union and UK markets, managing risk management plans, safety updates, and regulatory intelligence.
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Safety Aggregate Report Coordinator Associate PfizerPoland - Warsaw PLN 101k8d Project management of safety aggregate reports submitted to regulators (FDA, EMA) to ensure timely completion and regulatory compliance.
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Safety & PV Submission Spec I - Brazil Home Based↗ Syneos HealthRemote 8d Assisting with the design, preparation, and assembly of expedited and periodic safety reports for regulatory authorities, ethics committees, and investigators in clinical trials and post-marketing safety programs.
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