Pharmacovigilance
501 open positions
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Client Dedicated Safety Writer II ThermofisherRemote, Serbia 8d Plan, coordinate, and deliver safety writing services for clinical trial and marketed product projects in a regulated pharmacovigilance environment.
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Pharmacovigilance Intake Specialist BaxterWarsaw, Masovian, PL PLN 112k8d 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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Scientific Director (SERM & Clinical Safety & Pharmacovigilance) - Remote - Based in India↗ Alphanumeric SystemsRemote 8d Provide scientific leadership in product safety evaluation, benefit-risk management, and pharmacovigilance across clinical and post-marketing programs.
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Manager, PST Program Management AbbVieNorth Chicago, IL, us 8d 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 9d 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 9d 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 9d Own the product roadmap and technology strategy for signal detection, benefit-risk, and risk management platforms supporting global pharmacovigilance operations.
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Medical Safety Dir IqviaBangalore, India 9d Provide global medical expertise and oversight for pharmacovigilance services, including adverse event review, regulatory reporting, and safety profile management across clinical trials and post-marketing projects.
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Clinical Trial Manager↗ SciproMunich, Bavaria, Germany 9d 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 9d Support Pharmacovigilance activities for the European Union and UK markets, managing risk management plans, safety updates, and regulatory intelligence.
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Safety & PV Submission Spec I - Brazil Home Based↗ Syneos HealthRemote 9d 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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Safety Aggregate Report Coordinator Associate PfizerPoland - Warsaw PLN 101k9d Project management of safety aggregate reports submitted to regulators (FDA, EMA) to ensure timely completion and regulatory compliance.
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Medical Officer Class 3 (MO3) – Clinical Evaluator HudsonCanberra Region, Australian Capital Territory 10d Conduct evidence-based evaluations of complex clinical trial data and scientific dossiers to guide the approval and registration of prescription medicines in Australia.
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Head Medical Safety Assessment and External Engagement↗ Novartis India 10d Overseeing the quality of medical review of safety cases in the Novartis Safety system, managing external service providers, and organizing deliverables for Medical Safety Experts.
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Local Contact Person for Pharmacovigilance (LCPPV) - Freelance↗ Allucent 10d Coordinates and performs logistical aspects of pharmacovigilance activities in post-marketed programs to ensure compliance with local requirements.
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Senior Support Engineer - Life Sciences/Safety Products (Argus or Empirica)↗ Oracle 11d Primary technical support point of contact for Oracle Life Sciences Safety products (Argus/Empirica), troubleshooting issues to ensure patient safety and regulatory compliance.
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Pharmacovigilance Associate↗ Sentrex Health SolutionsMarkham, Ontario, Canada $60k11d Managing the collection, processing, and reporting of Adverse Events (AEs) and Product Complaints in compliance with Health Canada regulations and GxP standards.
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Director, PV Clinical Operations↗ Takeda PharmaceuticalsCambridge, MA, US $177k–$278k11d Provide functional expertise and program-level oversight of outsourced pharmacovigilance activities across clinical trials, including study setup, CRO training, and vendor management.
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Senior Pharmacovigilance Scientist (Vaccines/ Products of National Significance) CSL PlasmaAustralia 12d Lead safety review, signal detection, and risk management for CSL vaccines and products of national significance across their lifecycle.
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Senior Specialist, Drug Safety MsdPOL - Mazowieckie Wojewodztwo - Warsaw (Trade Center), PL 12d Develop and maintain processes for high-quality individual case and aggregate safety reporting in accordance with pharmacovigilance (PV) policy and regulations.
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Senior Manager, PVRM Safety Scientist SumitomopharmaRemote $157k–$196k12d Lead Pharmacovigilance and Risk Management (PVRM) activities, serving as the primary safety point of contact for assigned oncology and neurology programs to ensure safety governance and benefit-risk evaluation.
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Manager Global Case Management Submissions↗ OtsukaRemote, US $121k–$181k12d Manage global adverse event reporting and submissions for medicinal and device products to ensure compliance with international regulations.
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Senior Manager, PVRM Safety Scientist↗ Sumitomo GroupRemote $157k–$196k12d Lead Pharmacovigilance and Risk Management (PVRM) activities, serving as the primary safety point of contact for assigned oncology and neurology programs to ensure patient safety and regulatory compliance.
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Deputy Manager- Medical Reviewer PV Operations↗ ViatrisBengaluru, Karnataka, India 12d Perform medical review and assessment of Individual Case Safety Reports (ICSRs) for both Drug (PV) and Non-Drug (NDR) vigilance, ensuring compliance with global regulatory requirements.
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Assoc I PSS↗ FortreaRemote 12d Process and manage adverse event reports from clinical trials and post-marketing settings, ensuring compliance with regulatory timelines and standards.
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Medical Evaluator - Global Case Management↗ CslMelbourne, Victoria, Australia 12d Oversee vendor medical evaluation activities and provide expert guidance on complex Individual Case Safety Reports (ICSRs) to ensure high-quality safety assessments.
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Director, Medical Safety Assessment Physician BristolmyerssquibbPrinceton - NJ - US 12d Lead safety activities, benefit-risk strategies, and signal evaluation for assigned pharmaceutical compounds throughout the drug lifecycle.
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Director, Medical Safety Assessment Physician BmsPrinceton - NJ - US 12d Lead global medical safety activities, benefit-risk strategies, and regulatory safety submissions for assigned pharmaceutical compounds.
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Senior Director, Global Patient Safety - Rare Disease RegeneronWarren, US $242k–$403k12d Lead global patient safety strategy, signal management, and benefit-risk assessment for obesity/metabolism products in various development stages.
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Senior Scientist, Risk Management & Safety Surveillance ClinChoiceUnited States 12d Senior scientist responsible for aggregate safety reports, case-level reviews, and safety strategy development for pharmaceutical products.
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Senior Manager, Safety Cluster Lead PeopleservicesAU Sydney 13d Lead local Pharmacovigilance (PV) operational activities across multiple territories, managing vendor partnerships and ensuring regulatory compliance for patient safety.
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Medical Monitor↗ Accelagen Pty LtdSydney, New South Wales, Australia 13d Oversee safety aspects of clinical trials from design to close-out, acting as the medical reference for study teams and investigative sites.
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Lead Pharmacist - Medication Safety↗ SA HealthAdelaide, SA, AU $123k13d Lead the establishment, management, and leadership of a sustainable statewide medicines safety program, coordinating analysis of medicines safety incident learnings and developing strategies for statewide practice improvements.
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Senior Manager, Safety Cluster Lead↗ MundipharmaSydney, New South Wales, Australia 13d Lead local Pharmacovigilance (PV) operational activities across multiple territories, ensuring regulatory compliance and patient safety for a global pharmaceutical organization.
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