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Healthcare
› Pharmacovigilance
Pharmacovigilance
334 open positions
Technical Consultant
Eversana
Pune, MH, in
1d
Configure, maintain, and optimize Oracle Argus Safety to support pharmacovigilance operations, regulatory reporting, and data migration projects.
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Medical Safety Industrial Student Placement
Kenvue
Europe/Middle East/Africa, United Kingdom, Reading, Berkshire
1d
12-month industrial placement for university students to gain practical experience in medical safety functions including adverse event management, signal detection, and risk management.
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Safety Aggreg Report Mng /Senior PV Scientist
Iqvia
Belgrade, Serbia
1d
Lead global functional roles for Safety Aggregate Reports and Analytics (SARA) deliverables, including aggregate reporting, literature surveillance, and signal management for marketed and investigational products.
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LPN- Adverse Drug Events- Remote
Cigna
Remote
1d
Review, document, and submit adverse drug event reports to pharmaceutical manufacturers and the FDA to ensure patient safety and regulatory compliance.
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Associate Director, Global Patient Safety Standards & Training
Regeneron
Uxbridge1, GB
1d
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
Bristolmyerssquibb
Princeton - NJ - US
$218k–$218k
1d
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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Pharmacovigilance Associate
Gsk
Petach Tikvah, IL
1d
Support the pharmacovigilance team in Israel by ensuring safety data and systems are accurate and compliant, processing safety information, and supporting reporting activities.
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Medical Director, Safety Sciences
↗
Denali Therapeutics
South San Francisco, CA, US
$272k–$272k
1d
Senior clinical leadership for safety strategy, oversight, and benefit-risk evaluation across multiple development programs or a therapeutic area.
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Associate Medical Director (Psychiatry)
↗
Iqvia
Remote
1d
Acts as a global and regional Medical Advisor providing medical support to investigative sites and project staff for protocol-related issues, patient safety, and eligibility determinations in clinical trials.
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Senior Medical Director, Pharmacovigilance and Safety
Oruka Therapeutics
Remote
$306k–$306k
2d
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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サ
Safety Physician (MBBS) | Pharmacovigilance Medical Review | Immediate Joiners Preferred
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サイネオス・ヘルス
TS, IN
2d
Performs medical review of adverse events for investigational and marketed products, ensuring medical accuracy of case narratives and coding.
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Safety Physician (MBBS) | Pharmacovigilance Medical Review | Immediate Joiners Preferred
↗
Syneos Health
TS, IN
2d
Performs medical review of adverse events for investigational and marketed pharmaceutical products to ensure appropriate interpretation and regulatory compliance.
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Pharmacovigilance Officer - DEMO Global Services
Demo S.A.
Hyderabad, Telangana
3d
Perform global literature screening, review, assess, process, and record Individual Case Safety Reports (ICSRs) for a diverse portfolio of medicinal products.
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Senior Specialist or Manager, Pharmacovigilance, Oncology
AbbVie
Minato City, Tokyo, jp
3d
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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Associate Manager - PV Case Processing
Elanco
Bangalore, Karnataka
3d
Assess, manage, and submit adverse event reports in compliance with global pharmacovigilance regulations.
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Senior Safety Reporting Coordinator
↗
Thermo Fisher Scientific
Desde casa, MX
3d
Administrative safety support for Pharmacovigilance department, managing submissions, tracking, filing, and archiving of expedited and periodic safety reports.
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Drug Safety Specialist
Avance Clinical
Melbourne, Victoria
3d
Provide drug safety reporting and management services for clinical trials, ensuring compliance with protocols and regulations.
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Associate Director, PV Document Management Oversight
2028 Takeda Innovations India
India
3d
Lead the development and oversight of global aggregate safety reports (PSURs, NOAs) and risk management plans for investigational and marketed pharmaceutical products.
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Associate Director, Clinical Trial Patient Safety
AbbVie
North Chicago, IL, us
4d
Manage worldwide surveillance of clinical trial patient safety data, ensuring compliant and timely adverse event monitoring and review for assigned compound studies.
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Senior Medical Director, Immunology, Global Patient Safety
AbbVie
North Chicago, IL, us
4d
Lead global patient safety and pharmacovigilance activities for immunology products, ensuring safety through surveillance, signal detection, and risk management.
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Senior PV Officer
PrimeVigilance
Pune, Maharashtra
4d
Managing Individual Case Safety Reports (ICSRs) and safety data for clinical trials in compliance with pharmacovigilance regulations.
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Drug Safety Associate - Bilingual - French
↗
Cencora
Toronto, ON, CA
4d
Receive, scan, document, and triage clinical information, adverse events, and product quality complaints for Cencora's patient and provider support and pharma commercialization services in Canada.
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Associate Director, Quality Auditor, GVP
Gsk
Remote
4d
Lead independent global pharmacovigilance audits and drive quality compliance strategies across R&D to ensure adherence to international regulations and GSK standards.
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External Vigilance Engagements Lead
Novartis
Hyderabad (Office), IN
4d
Lead external vigilance engagements and manage contractual arrangements for pharmacovigilance and device vigilance across Novartis Enterprise, including M&A transitions and partner compliance.
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External Vigilance Engagements Lead
↗
Novartis
TS, IN
4d
Provide expertise and cross-functional leadership on pharmacovigilance and device vigilance for Novartis Enterprise contractual arrangements, managing external vigilance agreements and leading transition projects for M&A and strategic initiatives.
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Medical Director / Senior Medical Director, Psychiatry
Thermofisher
Remote, Texas, USA
4d
Provides medical oversight of clinical trials in Psychiatry to ensure adherence to SOPs, client directives, GCP, and regulatory requirements.
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Drug Safety Associate - Bilingual - French
Myhrabc
CAN > ON > Remote, CA
4d
Receive, 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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FSP Quality Manager
↗
Thermo Fisher Scientific
Remote, GB
4d
Operational execution of the Pharmacovigilance (PV) Quality Management System (QMS) to ensure consistent, effective, and efficient patient safety standards.
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Pharmako- / Vigilanzmanager*in in klinischen Studien (stellvertretende Fachbereichsleitung) (m/w/d)
↗
Universitätsklinikum Freiburg
Remote
$0k–$0k
4d
Lead pharmacovigilance operations for clinical trials, managing safety reporting and regulatory compliance for the University Hospital Freiburg.
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Senior Manager, Kite Safety and Pharmacovigilance
Gilead
United States - California - Foster City
$169k–$169k
4d
Provide scientific and strategic leadership for pharmacovigilance activities supporting investigational and marketed CAR T-cell cancer therapies.
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Drug Safety Associate
↗
Cencora
Toronto, ON, CA
4d
Receive, 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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FSP Quality Manager
Thermofisher
Remote, United Kingdom
4d
Operational execution of the Pharmacovigilance (PV) Quality Management System (QMS) to ensure consistent, effective, and efficient patient safety operations.
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Senior PV Officer
Ergomed
Pune, MH, in
5d
Senior Pharmacovigilance Officer managing Individual Case Safety Reports (ICSRs), safety data reconciliation, and acting as Local Contact Person for Pharmacovigilance (LCPPV) and Person Responsible for Local Screening (PRLS) for specific countries/languages.
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Senior Scientist, Risk Management & Safety Surveillance
Jobgether
Remote
$80k–$80k
5d
Leading pharmacovigilance activities to assess medicine safety and benefit-risk profiles, including aggregate safety reports, signal evaluation, and regulatory responses.
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Medical Advisor
Ministry of Health – Manatū Hauora
New Zealand
$130k–$130k
5d
Evaluate clinical trial data and scientific information to determine if medicine benefits outweigh risks, and regulate medicines in use.
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Associate Regulatory Affairs Quality, Standards & Training Director (Global Patient Safety )
Jobgether
Remote
$163k–$163k
5d
Provides compliance oversight across Global Patient Safety and Regulatory Affairs, monitoring indicators, inspection-readiness, and operational performance for clinical programs.
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Senior Director of ICSR
Ergomed
Belgrade, rs
5d
Manages the ICSR Management Unit, overseeing staff, resources, and processes to ensure high-quality pharmacovigilance case processing and productivity.
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Senior Director of ICSR
Ergomed
Zagreb, hr
5d
Manages the ICSR Management Unit, overseeing staff, resources, and processes to ensure high-quality pharmacovigilance case processing and patient safety reporting.
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Patient Safety PVSci Manager
Vrtx
Remote
$121k–$121k
5d
Leads pharmacovigilance science activities including cross-functional safety data monitoring, aggregate reporting to regulatory agencies, and signal/risk management for assigned products.
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Global Patient Safety and Pharmacovigilance Industrial Placement, UK 2027
Gsk
UK – London – New Oxford Street
$29k–$29k
5d
Support Global Safety teams in monitoring medicine safety, collecting and analyzing adverse event data, and assisting in benefit-risk assessments for clinical trials and post-marketing.
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PV Coordinator
Thermofisher
Remote, Bulgaria
5d
Lead project coordination and safety support for global and domestic clinical programs, focusing on adverse events, protocol inquiries, and Data and Safety Monitoring Boards.
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Medical Director/Senior Medical Director - Endocrinology(Remote U.S)
↗
Thermo Fisher Scientific
Remote
$200k–$200k
5d
Provides medical oversight of clinical trials to ensure safety profiles, regulatory compliance, and accurate medical content for new drug development.
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Pharmacovigilance Specialist
Iqvia
Remote
5d
Review, assess, and process safety data and information across service lines, including collecting and tracking incoming Adverse Events (AEs), database entry, coding, and writing narratives.
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Scientific Director, Immunology, Global Patient Safety
AbbVie
North Chicago, IL, us
6d
Leads the development and implementation of safety strategies for immunology assets throughout the drug lifecycle, ensuring medical accuracy and scientific rigor in regulatory and clinical documents.
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Senior Benefit/Risk Associate
Ergomed
Belgrade, rs
6d
Performing and supporting contracted pharmacovigilance activities, specifically signal detection, evaluation, and reporting to ensure patient safety.
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Medical Director/Senior Medical Director - Endocrinology(Remote U.S)
Thermofisher
Remote
$200k–$200k
6d
Provides medical oversight of clinical trials to ensure safety profiles, regulatory compliance, and accurate medical content for drug development.
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Lead Pharmacist Contact Center Specialist
Denverhealth
Rocky Mountain Poison & Drug Safety - 1391 Speer Blvd, Denver, CO 80204, US
$110k–$110k
6d
Provides medical information, collects safety reports, and manages product complaints for consumers, patients, and healthcare providers.
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FSP Pharmacovigilance Coordinator (Night Shift)
Thermofisher
Remote, Philippines
6d
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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Specialist, Drug Safety
Msd
EGY - Cairo - Cairo (New Cairo), EG
6d
Manage pharmacovigilance intake, prepare and submit Individual Case Safety Reports (ICSRs) and aggregate safety reports, and support audits/inspections to ensure regulatory compliance and patient safety across the Middle East.
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Medical Information Specialist I - Nurse
Thermofisher
Morrisville, North Carolina, USA
6d
Provide technical and medical information, intake adverse events, and manage product complaints for pharmaceutical and device products.
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