Pharmacovigilance
491 open positions
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Medical Monitor, Rheumatology, Canada or Argentina InderoBuenos Aires, Argentina 1mo Provides medical and scientific support to clinical research programs in rheumatology, ensuring data integrity and subject safety oversight.
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Clinical Safety Manager - Pharmacovigilance / Drug Safety MedpaceLondon, United Kingdom 1mo Manage clinical safety activities, case management, and aggregate reporting for multiple large programs in the pharmacovigilance process.
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Associate Medical Director (PS-MD) AbbVieNorth Chicago, IL, us 1mo 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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Patient Safety Associate - 14-month contract Boehringer IngelheimSydney, New South Wales 1mo Manage Individual Case Safety Reports (ICSRs) and Safety Issue reporting to ensure regulatory compliance and patient safety for medicines across Australia and New Zealand.
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Senior Manager, Regulatory and PV Delivery PrimeVigilanceMelbourne, Victoria 1mo Senior Manager providing franchise liaison between Ergomed Group and clients, managing complex regulatory projects, and securing new business.
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Senior Director: Global Patient Safety Solutions Partner RegeneronWarren, US 1mo Orchestrates Digital & Technology capabilities to deliver Regeneron's Global Patient Safety objectives across platforms like Argus, PIVIT, and Signal Management.
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Vaccines Safety Sciences Lead CSL PlasmaMelbourne, Victoria 1mo Leads global pharmacovigilance (PV) safety sciences functions, ensuring regulatory compliance, managing safety data analysis, and overseeing PV system implementation for biotherapeutics.
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PV Auditor - Freelance Position ErgomedRemote 1mo 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 1mo 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 1mo Support the handling of Individual Case Safety Reports (ICSR) in the GEHC Global Adverse Event Database (GAED) in compliance with regulatory standards.
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Global Safety Program Lead/Sr Medical Director AstraZenecaBoston, Massachusetts, United States of America $281k–$421k1mo Lead global safety strategy, delivery, and oversight for assigned pharmaceutical assets, managing a team of safety physicians and scientists to optimize benefit-risk profiles.
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Gestionnaire principal(e), Pharmacovigilance Corporative/ Senior Manager, Corporate Pharmacovigilance↗ McKessonMontreal, Quebec, Canada 1mo Strategic and operational leadership of corporate pharmacovigilance and product safety programs for McKesson Canada, ensuring compliance with Canadian and international regulations for pharmaceuticals, natural health products, and medical devices.
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Senior Director, Safety Physician Amylyx PharmaceuticalsRemote 1mo Provide medical and scientific leadership for the evaluation of safety profiles and benefit-risk of investigational and commercial products across the product lifecycle.
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Senior Medical Director ThermofisherRemote 1mo Provide medical support, advice, and monitoring for clinical trials and safety evaluation within the Pharmacovigilance department.
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Global PV Partnership & Operations Director SobiBasel, BS, ch 2mo 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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Manager, Pharmacovigilance and Medical Information BiibhrParis, France 2mo Ensure patient safety and regulatory compliance for Biogen's biosimilar portfolio globally and local PV activities in France.
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Senior Director, US Risk Management & Product Safety (REMS) NovartisEast Hanover $204k–$380k2mo Lead US safety strategy for a portfolio of complex medicines, overseeing REMS design, FDA engagement, and risk management execution.
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Manager, Patient Safety, Epidemiology Science and Execution BristolmyerssquibbWarsaw - PL 154k2mo Execute post-marketing safety study components and contribute to regulatory-grade science to ensure medicine safety for patients.
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Senior Director, Global Safety Physician MadrigalpharmaPA - Conshohocken - Office $318k2mo Lead global clinical safety strategy, signal detection, and benefit-risk evaluation for investigational and marketed biopharmaceutical products.
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Director, Medical Safety↗ IqviaRemote 2mo Lead global medical safety and pharmacovigilance oversight for clinical and post-marketing programs, conducting medical reviews of safety data and regulatory reports.
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(Senior) Director, Drug Safety and Pharmacovigilance Operations AbCelleraVancouver CA$160k2mo Spearhead the evolution of the drug safety framework for Phase 3 clinical programs, ensuring regulatory compliance and paving the way for successful filings and commercial launch.
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Senior Consultant - Veeva Vault Safety - Japan & PMDA VeevaRemote 2mo Senior consultant leading implementation of Veeva Vault Safety for biopharmaceutical customers in Japan, acting as a subject matter expert for drug safety and pharmacovigilance.
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Clinical Medical Monitor PraxisprecisionmedicinesRemote $260k2mo Provide hands-on medical oversight for clinical programs, ensuring patient safety and study quality by supporting investigators and sites with medical guidance, safety assessments, and data surveillance.
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Scientist/Senior Scientist – QPPV Office, Local Safety Support & Regulatory Intelligence ClinChoicePhilippines - Pasig 2mo Safety expert providing oversight for the Consumer portfolio of products throughout their life cycle, including new product development, by evaluating safety data and managing risks.
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Manager, Global ICSR Management↗ BeOne MedicinesRemote 2mo Oversees triage, case processing, and quality control of Individual Case Safety Reports (ICSR) to ensure efficiency, quality, and compliance in drug safety operations.
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