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Healthcare
› Pharmacovigilance
Pharmacovigilance
494 open positions
Medical Monitor (Gastroenterologist)
Psi-Cro
Remote
1mo
Provides medical input to global clinical studies, focusing on patient safety, regulatory interactions, and therapeutic expertise in gastroenterology.
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Manager, Regulatory Affairs & Pharmacovigilance, Central EPM
Medison Pharma
București, Romania
1mo
Oversee regulatory and pharmacovigilance operations for Romania, Moldova, Hungary, Czech Republic, and Slovakia to ensure compliance with local and international requirements.
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Medical Director, Patient Safety Physician
AstraZeneca
India - Bangalore
1mo
Lead clinical safety strategy for high-impact therapies from development through post-marketing, guiding benefit-risk decisions and risk minimization to ensure patient protection and regulatory success.
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Senior Pharmacovigilance Specialist – Belgium and Luxembourg M/F/D
Msd
BEL - Brussels - Brussels (Souverain), BE
1mo
Managing daily pharmacovigilance activities, adverse event case management, and risk minimization for Belgium and Luxembourg markets.
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Senior Pharmacovigilance (PV) Clinical Scientist
Roche
South San Francisco, US
$121k
1mo
Lead clinical review and medical evaluation of Individual Case Safety Reports (ICSRs) to ensure regulatory compliance and patient safety.
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Director, Pharmacovigilance
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Rigel Pharmaceuticals, Inc.
South San Francisco, CA, US
$265k
1mo
Strategic and operational leadership for drug safety and pharmacovigilance, ensuring regulatory compliance, safety strategy, and risk management for a precision oncology portfolio.
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Global Head, Medical Drug Safety & Pharmacovigilance
Neurocrine
US CA San Diego
1mo
Global Head leading medical safety and benefit-risk strategy across Neurocrine's global development pipeline and marketed portfolio.
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SERM Medical Director
Gsk
UK – London – New Oxford Street
€410k
1mo
Provides medical and scientific leadership in the safety evaluation and risk management of GSK's oncology assets in clinical development.
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Safety Specialist/Safety Lead
Precisionmedicinegroup
Remote (Japan)
1mo
Manage clinical trial safety data, process serious adverse events (SAEs), and generate safety reports for sponsors and clients.
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Global Product Safety Science Lead
Sobi
Basel, BS, ch
1mo
Lead signal detection, benefit-risk evaluations, and safety strategy for assigned pharmaceutical products across the lifecycle.
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Pharmacovigilance - Team Lead
↗
Cognizant
1mo
End-to-end safety oversight across pharma R&D, coordinating PV data management and case processing to ensure accurate reporting, regulatory compliance, and continuous risk evaluation.
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Senior/Principal Drug Safety Specialist (Night Shift)
Thermofisher
Remote, Philippines
1mo
Senior/Principal Drug Safety Specialist performing Pharmacovigilance (PV) activities to ensure patient safety and operational excellence in a highly regulated pharmaceutical environment.
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Medical Director, Neuroimmunology, Global Patient Safety
AbbVie
North Chicago, IL, us
1mo
Oversee comprehensive safety surveillance for neuroscience products throughout their lifecycle, including signal management and pharmacovigilance activities.
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Senior Pharmacovigilance Manager, Sydney
On Q Recruitment
Sydney, New South Wales
1mo
Lead Pharmacovigilance operations across Australia and New Zealand, ensuring regulatory compliance and patient safety excellence while building organizational capability.
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Senior Medical Safety Scientist
Acadia Pharmaceuticals
Princeton, New Jersey, United States; San Diego, California, United States
$145k
1mo
Scientific safety expert leading pharmacovigilance, signal detection, and benefit-risk evaluations for assigned products across the product lifecycle.
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Global Pharmacovigilance (PV) Scientist, Manager- Oncology
Amgen
United States - Remote
1mo
Lead product safety surveillance, signal management, and aggregate safety reporting for oncology and immunology products across the product lifecycle.
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Global Safety Medical Director, Rare Disease
Amgen
Remote
1mo
Strategic safety leader for Rare Disease assets, accountable for benefit-risk profile, signal management, and safety governance in early clinical development (Phase 1b/2).
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Principal Medical Writer
Gsk
Mississauga Milverton Drive, CA
$118k–$168k
1mo
Lead end-to-end authoring of complex clinical and post-market safety documents (e.g., DSURs, RMPs) for regulatory use, translating safety data into clear outputs.
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Manager, SDM China Lead
Msd
CHN - Beijing - Beijing (Wangjing Park), CN
1mo
Manage ICSR case management teams, medical coding, and operational oversight for Safety Data Management (SDM) processes, ensuring compliance with global regulations and quality standards.
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Director, Pharmacovigilance Hub - Americas
Regeneron
Cambridge, US
$183k
1mo
Oversee country and regional pharmacovigilance execution, ensuring local safety activities meet global standards and regulatory requirements while integrating data into the global PV system.
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Alnylam Pharmaceuticals – Safety and Risk Management Postdoctoral Research Fellow
Northeastern
Boston, MA (Main Campus), US
$60k
1mo
Postdoctoral Research Fellow in Safety and Risk Management supporting Alnylam's RNAi therapeutics platform.
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Manager, SDM China Lead
Msd
CHN - Beijing - Beijing (Wangjing Park), CN
1mo
Manage ICSR case management teams and encoding operations, ensuring operational readiness, quality, and compliance in safety data intake, triage, and analysis.
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Director, Head of PV and REMS Compliance
Bristolmyerssquibb
Princeton - NJ - US
$218k
1mo
Leading Patient Safety quality and compliance on all key processes through proactive, risk-based oversight and continuous monitoring of safety outputs, ensuring sustained compliance with global GVP regulations and FDA requirements for REMS programs.
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Associate Director, Global Patient Safety Standards & Training
Regeneron
Uxbridge1, GB
1mo
Establish and maintain Pharmacovigilance (PV) procedures and policies to ensure regulatory compliance and operational efficiency globally.
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Director, Head of PV and REMS Compliance
Bms
Princeton - NJ - US
$218k–$264k
1mo
Leading Patient Safety quality and compliance on all key processes through proactive, risk-based oversight and continuous monitoring of safety outputs, ensuring sustained compliance with global GVP regulations and FDA requirements for REMS.
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Senior Medical Director, Pharmacovigilance and Safety
Oruka Therapeutics
Remote
$306k
1mo
Lead medical and scientific safety oversight for investigational biologics targeting chronic skin diseases, ensuring compliance with global regulations and protecting participant safety.
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Senior Specialist or Manager, Pharmacovigilance, Oncology
AbbVie
Minato City, Tokyo, jp
1mo
Leading a team of PV operations to execute day-to-day operations and compliance activities for maintaining high-functioning PV systems across the assigned region remit, specifically for oncology products in Japan.
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Drug Safety Specialist
Avance Clinical
Melbourne, Victoria
1mo
Provide drug safety reporting and management services for clinical trials, ensuring compliance with protocols and regulations.
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Senior Medical Director, Immunology, Global Patient Safety
AbbVie
North Chicago, IL, us
1mo
Lead global patient safety and pharmacovigilance activities for immunology products, ensuring safety through surveillance, signal detection, and risk management.
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FSP Quality Manager
Thermofisher
Remote, United Kingdom
1mo
Operational execution of the Pharmacovigilance (PV) Quality Management System (QMS) to ensure consistent, effective, and efficient patient safety operations.
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Director, Patient Safety Physician - Cardio Renal Metabolic
↗
Boehringer Ingelheim
Remote
$265k
1mo
Provide strategic medical safety leadership for investigational compounds across early clinical development, translating evidence into benefit-risk decisions.
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Senior Director, EEA Deputy QPPV (m/f/d)
Bms
Vienna - AT
1mo
Acts as the primary point of contact for pharmacovigilance oversight in the EEA, ensuring compliance with regulatory obligations and managing safety profiles for assigned products.
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Senior Benefit/Risk Associate
Ergomed
Belgrade, rs
1mo
Performing and supporting contracted pharmacovigilance activities, specifically signal detection, evaluation, and reporting to ensure patient safety.
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FSP Pharmacovigilance Coordinator (Night Shift)
Thermofisher
Remote, Philippines
1mo
Coordinate pharmacovigilance safety support and project management for global and domestic clinical programs, managing adverse events, DSMB/EAC meetings, and contractual documentation.
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Medical Director/Senior Medical Director - Endocrinology(Remote U.S)
Thermofisher
Remote
$200k
1mo
Provides medical oversight of clinical trials to ensure safety profiles, regulatory compliance, and accurate medical content for drug development.
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Pharmacovigilance Associate
Icon
India, Chennai
1mo
Monitor and ensure the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information.
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Senior Scientist, Risk Management & Safety Surveillance
ClinChoice
Canada
1mo
Senior scientist responsible for aggregate safety reports, case-level reviews, and safety strategy development for pharmaceutical products.
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Senior Associate, Aggregate Reporting Physician
ClinChoice
Philippines - Pasig
1mo
Guide report strategy and review medical/safety content (signals, adverse events, benefit-risk assessments) for pharmaceutical safety reports.
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Senior Manager, Safety Scientist
AstraZeneca
Boston, Massachusetts, United States of America
$133k–$199k
1mo
Senior Manager leading global patient safety risk evaluation, regulatory reporting, and safety strategy execution across the product lifecycle.
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Temp Mgr Global Patient Safety Sciences
Regeneron
TARRYTOWN, US
1mo
Manage global patient safety strategies for molecules in clinical development and post-marketing phases, including safety data aggregation, review, analysis, and benefit-risk assessment.
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Senior Manager, Safety Scientist
AstraZeneca
US - Boston - MA
$133k
1mo
Lead global patient safety risk evaluation and management across the product lifecycle, ensuring compliance with GxP and global regulations.
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Principal Medical Safety Specialist
Bostonscientific
Arden Hills US-MN, United States | US-MN-Arden Hills, US-MA-Marlborough
$102k–$194k
1mo
Principal Medical Safety Specialist responsible for medical review of adverse event data and safety signal evaluation for cardiology, electrophysiology, and LAAO products.
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Senior Patient Safety Physician
↗
Boehringer Ingelheim
Ingelheim am Rhein, Rhineland-Palatinate, Germany
1mo
Lead global patient safety strategy and shape the development of innovative medicines by driving benefit-risk assessments and patient safety strategies for compounds in development and marketed products.
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Executive Medical Director, SERM
Sarepta
Cambridge, MA
$313k
1mo
Lead safety scientists and physicians to oversee pharmacovigilance, risk management, and safety data analysis for investigational and marketed products in muscle, CNS, and cardiac disease programs.
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Principal Investigator (Virtual)
Careaccess
Remote
$200k
1mo
Provide overall medical oversight and review of clinical trial protocols, safety reports, and case report forms to ensure participant safety and regulatory compliance.
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Associate Director, Global Patient Safety Standards & Training
Regeneron
Warren, US
$157k
1mo
Establish and maintain Pharmacovigilance (PV) procedures and policies to ensure global regulatory compliance and operational efficiency.
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Senior Manager, Global Patient Safety - General Medicine
Regeneron
Uxbridge1, GB
1mo
Lead scientific safety strategies for molecules in clinical development and post-marketing phases, including data aggregation, review, analysis, and benefit-risk assessment.
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Sr Safety Reporting Specialist
ThermoFisher Scientific
Brasil
1mo
Lead and oversee the preparation of complex safety reports, ensure compliance with international pharmacovigilance regulations, and drive continuous improvement in reporting processes to safeguard patient health.
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Executive Director - Clinical Research Physician - GPS Medical
Lilly
São Paulo, Estado de São Paulo
1mo
Lead the development, management, execution, and oversight of safety programs for therapeutic assets throughout their life cycle, acting as the GPS Medical representative for internal and external stakeholders.
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Vice President, Medical Affairs
Indero
Montreal, Canada
1mo
Lead unified Medical Monitoring and Pharmacovigilance functions with P&L accountability, driving strategic direction, business development, and safety standards for a global CRO.
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