Pharmacovigilance
356 open positions
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AI Consultant - Pharmacovigilance/Safety Systems Implementation↗ Veeva SystemsRemote $70k–$70k1mo Advise life sciences clients on implementing, validating, and governing AI agents within Vault Safety workflows to ensure compliance with GxP and FDA/EMA regulations.
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QA SENIOR MANAGER↗ AlmirallSant Feliu de Llobregat, Catalonia, Spain 1mo Maintain, develop, and continuously improve the Almirall GVP Quality Management System to ensure compliance with regulations and guidelines for pharmacovigilance activities.
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Research Safety Reporting Specialist (DOM Infectious Disease) JhuBaltimore, MD, United States $54k–$54k2mo Manage safety reporting, adverse event reviews, and regulatory compliance for multi-centered clinical trials in solid organ transplantation and infectious diseases.
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Associate Medical Director, Safety Evaluation and Risk Management (SERM) GskRemote $87k–$87k2mo Provide medical/scientific expertise in safety evaluation and risk management for GSK assets in clinical development and post-marketing settings.
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Pharmacovigilance Regulatory Reporting (Trilingual)↗ IqviaRemote 2mo Submit safety reports to regulatory authorities by reviewing, assessing, and processing safety data from various sources.
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Alternance - Pharmacovigilance AstraZenecaFrance - La Defense 2mo Managing adverse event notifications, monitoring drug safety profiles, detecting safety signals, and ensuring proper medication use within AstraZeneca France.
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Senior Medical Project Coordinator, EMEA ThermofisherRemote, Bulgaria 2mo Manages, coordinates, and evaluates medical projects for clinical safety and monitoring programs, ensuring compliance and optimal performance throughout the project lifecycle.
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Post Market Surveillance (PMS) Specialist Medical Devices (m/f/d) NovantaBerlin, Germany 2mo Point of contact for medical/clinical issues responsible for vigilance, Post-Market surveillance (PMS), and Post-Market Clinical Follow-Up (PMCF) activities.
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PV Officer- Senior PV Officer, Team Leader (Pharmacovigilance Manager) ErgomedPrague, Prague, cz 2mo Senior Pharmacovigilance Team Leader managing ICSR staff, optimizing processes, and acting as Local Contact Person for Pharmacovigilance (LCPPV) and Person Responsible for Local Screening (PRLS) for specific countries/languages.
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Medical Director, Neuroscience, Global Patient Safety AbbVieNorth Chicago, IL, us 2mo Lead Product Safety Teams to monitor and characterize the safety profile of pharmaceutical, biological, and drug-device combination products throughout their lifecycle.
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Clinical Safety and Risk Management Associate Principal Scientist MsdCZE - Central Bohemian - Prague (Five), CZ 2mo Primary medical review of serious adverse experience reports to monitor and describe the safety profile of assigned pharmaceutical products.
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Drug Safety Specialist/ Clinical Safety Coordinator↗ MedpaceNavi Mumbai, Maharashtra, India 2mo Handling and processing adverse events from clinical trials and post-marketing surveillance sources.
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Clinical Research Safety Associate↗ Everest Clinical ResearchRemote $60k–$60k2mo Administrative and data management support for Data Monitoring Committees (DMCs) and clinical safety event processing in pharmaceutical trials.
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Product Expert – Safety & Medical GsknchIndia - Andra Pradesh - Hyderabad 2mo Owns the Safety and Medical technology ecosystem, ensuring compliant operations and enabling digital solutions for pharmacovigilance, adverse event management, and risk detection.
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Associate Pharmacokineticist I LabcorpBengaluru India 2mo Design and review study protocols, perform pharmacokinetic and toxicokinetic analyses, and prepare scientific reports for clients in the pharmaceutical and healthcare sectors.
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Medical Monitor (US Board-Certified Psychiatrist) Psi-CroRemote 2mo Provides medical input to global clinical studies, advises teams on patient safety, and manages trial-specific medical and safety-related questions.
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Director, Pharmacovigilance IconChina, Shanghai 2mo Oversee the safety and efficacy of pharmaceutical products throughout their lifecycle, leading pharmacovigilance and drug safety delivery across a portfolio.
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Pharmaziepraktikant*in Medical Affairs & Pharmakovigilanz für 2026 (alle Geschlechter)↗ BayerBerlin, Berlin, Germany $27k–$27k2mo Intern in Pharmacovigilance learning organizational structures, processes, and responsibilities for monitoring drug safety in a global company.
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[JDSU] 医薬品安全性統括部 ケースマネジメントチーム（一般社員） （Staff, Case Management, Japan Drug Safety Unit） PfizerJapan - Tokyo 2mo Collecting, assessing, and managing safety information (adverse events) for marketed and investigational Pfizer products while ensuring compliance with Japan, US, and EU regulations.
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Medical Director, MPMD, PSPV TakedaIND - Bengaluru 2mo Provide strategic and medical leadership for global patient safety across assigned pharmaceutical and biological products, acting as the Global Safety Lead accountable for end-to-end safety strategy and benefit-risk evaluation.
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Associate Director of Medical Information DenverhealthRocky Mountain Poison & Drug Safety - 1391 Speer Blvd, Denver, CO 80204 $143k–$143k2mo Design, oversee, and lead Medical Information Drug Center programs and services, ensuring quality, audit readiness, and compliance with ethical and regulatory requirements while delivering pharmacovigilance and medical affairs services.
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Medical Director - Pneumonologist (Client - dedicated), EMEA ThermoFisher ScientificNederland 3mo Provide medical leadership, safety evaluation, and protocol development for clinical trials in the pharmaceutical industry.
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Director. Global Clinical Safety Scientist MadrigalpharmaPA - Conshohocken - Office $213k–$213k3mo Lead safety scientist for assigned projects, developing and maintaining safety assessments for all Madrigal clinical products in conjunction with the CSPV Physician and cross-functional team members.
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Manager Patient Safety Italy SandozMilano, Provincia di Milano 3mo Lead pharmacovigilance activities for the Sandoz affiliate, ensuring local safety procedures are comprehensive, effective, compliant, and embedded in the global-regional-local environment.
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Drug Safety Associate Consultant ClinChoiceRemote 3mo Process adverse event cases through intake, triage, data entry, quality review, and finalization for pharmaceutical and medical device partners.
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PV Physician IreTrivandrum, Thiruvananthapuram 3mo Oversee medical aspects of pharmacovigilance activities to ensure the safety of investigational drugs and contribute to the advancement of innovative treatments.
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Senior Manager PV Sweden & Affiliate Safety Representative ViatrisSolna, Stockholm County, Sweden 3mo Organize, manage, and maintain a highly compliant Pharmacovigilance (PV) system for Viatris in Sweden, acting as the main contact for health authorities and leading the local PV team.
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Global Product Safety Science Lead SobiStockholm, Stockholm County, se 3mo Lead product-level safety ownership, signal detection, benefit-risk evaluations, and regulatory interactions for assigned pharmaceutical products.
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Pharmacovigilance Associate Position Puma Biotechnology, Inc.Los Angeles, Los Angeles, California, United States 3mo Process adverse events and special situation cases to ensure timely, accurate, and compliant Individual Case Safety Report (ICSR) intake, processing, reporting, and reconciliation.
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