Pharmacovigilance
491 open positions
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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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Medical Project Coord ThermofisherRemote, Mexico, BR 20d Coordinate and review safety data, monitor clinical trial status, and support drug safety operations to ensure regulatory compliance and patient safety.
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Manager, Drug Safety - ICSR Processes BiibhrResearch Triangle Park, NC, US $116k–$155k21d Define, design, maintain, and improve global Individual Case Safety Report (ICSR) process standards, conventions, and procedural documentation for clinical and post-marketing safety activities.
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Safety Project Manager IqviaDurham, North Carolina, United States of America 21d Manage and deliver large regional and global Lifecycle Safety projects (clinical trial and/or post-market) for customers in the life sciences industry, serving as the primary point of contact and solution architect.
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Director, Global Pharmacovigilance Operations Lead SareptaCambridge, MA, US $186k–$232k21d Oversee global pharmacovigilance (PV) case management activities for investigational and marketed products, leading strategic operational projects and initiatives.
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Principal Safety Operations Specialist - Quality Focused Syneos HealthIndia 22d Principal Safety Operations Specialist ensuring quality and compliance in Pharmacovigilance operations, supporting safety project teams with audit readiness and quality improvement initiatives.
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Medical Monitor, Dermatology, Europe InderoWarsaw, Poland 22d Provides medical and scientific support to dermatology clinical research programs, ensuring data integrity and subject safety oversight.
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Senior Manager, Pharmacovigilance EikontherapeuticsJersey City, New Jersey $170k22d Managing safety data and ensuring patient safety by monitoring adverse events and ensuring regulatory compliance for clinical-stage drug programs.
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Medical Director, Early Pipeline, Immunology, GPS AbbVieNorth Chicago, IL, us 22d Lead safety surveillance, signal detection, validation, assessment, and risk management for early development immunology products.
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PV Innovation & Transformation Consultant ExcelyaBelgië 22d Lead cross-functional transformation and innovation projects in Global Pharmacovigilance, optimizing safety workflows and data governance following the implementation of a new safety database platform.
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A07 Immediate Action Officer Public Sector PeopleQLD - Brisbane, Queensland 22d Lead a specialist team to assess high-risk complaints and determine if immediate regulatory action is needed to protect public health and safety.
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Manager, Patient Safety, Epidemiology Science and Execution BmsWarsaw-WeWork-PL 154k22d Execute post-marketing safety study components, draft regulatory-grade science documents, and coordinate cross-functional activities to ensure medicine safety.
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Drug Safety Officer↗ TfsLondon, ENG, GB 22d Manage drug safety and vigilance issues for clinical trials and market reports, ensuring compliance with regulatory requirements and company SOPs.
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Senior Manager, Pharmacovigilance Operations↗ Viridian TherapeuticsRemote 22d Lead day-to-day pharmacovigilance operational activities and vendor oversight across clinical trials for investigational therapeutics targeting autoimmune and rare diseases.
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PV Quality Assurance Manager (m/f/d)↗ ValnevaVienna, Vienna, Austria €52k22d Strategic role driving enhanced compliance throughout the Pharmacovigilance (PV) domain to support Marketing Authorization Holders and the QPPV in maintaining a Global PV system.
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Sr Associate Global Safety AmgenChina - Beijing 22d Conduct core safety activities including data collection, processing, distribution, and regulatory submission of adverse events and periodic safety reports within the local country to support Amgen Global Patient Safety and the local business.
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Wood Sander First Fit ShopfittersCape Town Region, Western Cape 23d Associate Medical Safety Director leading pharmacovigilance and risk management activities for a global medical safety team.
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Analista de Farmacovigilância Pleno MatrizSão Paulo, Estado de São Paulo 24d Process adverse event reports, conduct literature searches, and prepare risk management plans and benefit-risk assessment reports for pharmaceutical products.
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Pharmacovigilance Services Assoc Manager AccentureIndia 25d Lead medical review and safety surveillance for Individual Case Safety Reports (ICSRs) in the pharmaceutical industry, ensuring regulatory compliance and data accuracy.
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Senior Benefit/Risk Associate ErgomedWarsaw, Masovian Voivodeship, pl 25d Performing and supporting contracted pharmacovigilance activities, specifically signal detection, evaluation, and reporting to ensure patient safety.
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PV Associate Analytics & Reporting GaldermaBarcelona, ES 25d Perform routine global pharmacovigilance activities including aggregate reporting, signal detection, literature monitoring, and risk management for medicinal and cosmetic products.
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Global Safety Program Lead AstraZenecaGaithersburg, Maryland, United States of America 25d Lead the global safety strategy, delivery, and oversight for assigned pharmaceutical assets, managing a team of safety physicians and scientists to optimize benefit-risk profiles and ensure regulatory compliance.
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Drug Safety Associate↗ CencoraRemote 25d 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 Project Director EversanaYardley, PA, us $120k26d Primary client-facing pharmacovigilance director responsible for strategic oversight, operational governance, and delivery excellence across assigned client programs.
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Senior Pharmacovigilance Manager, Sydney OnQ RecruitmentSydney, New South Wales 26d Lead Pharmacovigilance operations and strategy for Australia and New Zealand, ensuring compliance and patient safety excellence.
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Assoc. Spclst, Drug Safety MsdIDN - Jakarta - Jakarta (Menara Astra), ID 26d Execute local pharmacovigilance (PV) activities including adverse event case management, safety reporting, and regulatory compliance for pharmaceutical products.
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Medical Monitor (US Board-Certified Gastroenterologist) Psi-CroRemote 27d Provides medical input to global clinical studies, advises teams on patient safety, and monitors trial participant safety.
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Lead GPV Professional, ICSR Conventions Teva PharmaceuticalsNavi Mumbai, Maharashtra 27d Lead GPV Professional ensuring regulatory compliance and inspection readiness for System Data Innovation (SDI) processes and Global Pharmacovigilance (GPV) conventions.
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Local Contact Person for Pharmacovigilance and Regulatory Affairs (Contractor) PrimeVigilanceBelgië 27d Local Country Person Responsible for Pharmacovigilance and Regulatory Affairs ensuring compliance with national requirements in Australia.
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Clinical Safety Coordinator MedpaceTokyo, Japan 27d Handling and processing adverse events from clinical trials and post-marketing surveillance sources.
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