Pharmacovigilance
354 open positions
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LOCAL CASE INTAKE ADVISOR AstraZenecaTaiwan 8d Manage the intake, processing, and communication of Individual Case Safety Reports (ICSRs) to safeguard patients and ensure regulatory compliance.
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Clinical Safety Manager - Pharmacovigilance / Drug Safety MedpaceLondon, United Kingdom 8d Manage clinical safety activities, case management, and aggregate reporting for multiple large programs in the pharmacovigilance process.
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Safety & PV Specialist JobgetherRemote 8d Process, track, and report Individual Case Safety Reports (ICSRs) to ensure patient safety and regulatory compliance across clinical and post-marketing programs.
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Associate Medical Director (PS-MD) AbbVieNorth Chicago, IL, us 9d Lead Medical Safety Review (MSR) of clinical trial Serious Adverse Events (SAEs), including causality assessment and company analysis development, while providing therapeutic area leadership.
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Sr Safety Specialist ThermofisherRemote, Mexico 9d Senior Safety Specialist performing Pharmacovigilance (PV) activities to ensure patient safety and operational excellence in a highly regulated pharmaceutical environment.
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Senior Director: Global Patient Safety Solutions Partner RegeneronWarren, US 9d Orchestrates Digital & Technology capabilities to deliver Regeneron's Global Patient Safety objectives across platforms like Argus, PIVIT, and Signal Management.
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PV Auditor - Freelance Position ErgomedRemote 9d Conducting Pharmacovigilance (PV) audits for pharmaceutical and biotechnology companies to ensure compliance with regulatory requirements and Good Pharmacovigilance Practice (GVP).
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Medical Information Specialist - German & English speaking EversanaRemote 10d Triage and respond to drug information inquiries from healthcare professionals and patients, identify adverse events, and perform medical writing.
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Drug Safety Intern, Global Case Processing GehcShanghai, CN 11d Intake, triage, data entry, quality review, coding, and follow-up of Individual Case Safety Reports (ICSR) in the Global Adverse Event Database (GAED) to ensure regulatory compliance.
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Directeur médical microbiologie et épidémiologie↗ Héma-QuébecRemote 11d Strategic oversight of emerging infectious diseases and biological risks to ensure the safety of the Quebec blood supply.
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Clinical/Medical Scientist (Medical Monitoring) - Infectious Disease↗ Syneos HealthRemote, US 11d Develop medical plans and perform regular medical reviews of clinical trial data to identify risks, trends, and data integrity issues for infectious disease studies.
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Lead Patient Safety Physician↗ Boehringer IngelheimBiberach an der Riß, BW, DE 11d Lead and provide medical-scientific direction to a global team of Patient Safety Physicians for late-stage cardiovascular, renal, and metabolic assets, ensuring patient safety and developing risk minimization strategies.
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Responsable Qualité / Vigilances FerringGentilly, France 11d Lead the local Quality and Pharmacovigilance strategy for Ferring France, ensuring regulatory compliance and patient safety for reproductive medicine, gastroenterology, urology, and oncology products.
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Manager, Safety Scientist↗ Beone MedicinesRemote 12d Manager, Safety Scientist supports assigned compounds in conjunction with Product Safety Leads to conduct signal detection, evaluation of safety data, assessment of safety risks, responses to regulatory inquiries, and regulatory-required periodic reporting.
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Pharmacovigilance Senior Assessor and Reporting Lead↗ Veterinary Medicines DirectorateNew Haw, ENG, GB 12d Lead post-authorisation surveillance of veterinary medicines in the UK, assessing benefit-risk balance and ensuring safety/efficacy throughout the product lifecycle.
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Senior PV Scientist BiibhrMaidenhead, United Kingdom 12d Lead safety signal management, aggregate reporting, and regulatory response for marketed products and clinical trials.
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Clinical Safety Specialist - Contractor↗ HrconnectedRemote $100k–$100k14d Collect, process, and oversee clinical trial safety data, including adverse event assessment and regulatory reporting.
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Global PV Partnership & Operations Director SobiBasel, BS, ch 14d Strategic leadership of the Sobi PV Partnership & Operations function, ensuring compliance and collaboration between internal teams, co-development partners, and external service providers for pharmacovigilance activities.
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Intern - Kite Development - Global Patient Safety GileadUnited States - New Jersey - Parsippany $0k–$0k15d Summer intern supporting pharmacovigilance and patient safety for CAR-T cell therapies, focusing on signal detection, aggregate safety analysis, and risk management.
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Senior Specialist Pharmacovigilance (Maternity Leave Cover) MsdBGR - Sofia City - Sofia (Nikola), BG 15d Execute local pharmacovigilance operations, manage adverse event case processing, and ensure regulatory compliance for patient safety.
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Associate Director, Global Patient Safety (GPS) Individual Case Safety Report (ICSR) Therapeutic Area (TA) Lead VrtxRemote $164k–$164k15d Oversees global Individual Case Safety Report (ICSR) processing excellence and external business management for a specific therapeutic area, ensuring adherence to pharmacovigilance regulations and managing vendor partners.
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Senior Safety Domain Expert - Falcon VeevaRemote 15d Senior Safety Domain Expert bridging hands-on pharmacovigilance case processing with strategic vision for AI and automation tools in Veeva Falcon.
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Pharmacovigilance Analyst↗ CognizantBuenos Aires, B, AR 16d Monitor, evaluate, and analyze drug safety data to ensure the safety and efficacy of pharmaceutical products while maintaining global regulatory compliance.
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Regulatory Affairs Manager FreseniusmedicalcareJakarta Selatan, JK 16d Manage regulatory compliance, submissions, and pharmacovigilance for medical devices and drugs in Indonesia.
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Senior Director, US Risk Management & Product Safety (REMS) NovartisEast Hanover $204k–$380k16d Lead US safety strategy for a portfolio of complex medicines, overseeing REMS design, FDA engagement, and risk management execution.
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Senior Manager, Clinical Data Analytics EdwardsUSA - California – Irvine $139k–$139k16d Design, validate, and maintain clinical safety dashboards and reports for internal stakeholders and safety governance bodies (e.g., DSMB, Safety Review Committee) within the Transcatheter Mitral and Tricuspid Therapies business unit.
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