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Healthcare
› Pharmacovigilance
Pharmacovigilance
329 open positions
Medical Director/Senior Medical Director - Rheumatology/Dermatology
Thermofisher
Remote, Argentina
23d
Provide medical oversight of clinical trials and marketed products, ensuring adherence to regulations and client directives while managing safety data and therapeutic expertise.
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Sr Pharmacovigilance Scientist
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Biogen
Cambridge, MA, US
25d
Lead signal management, author aggregate safety reports (PSURs, DSURs, REMS, RMPs), and manage safety inquiries for marketed products and clinical trials.
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Senior Medical Project Coordinator, EMEA
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Thermo Fisher Scientific
Remoto, PT
25d
Manages, coordinates, and evaluates medical projects for clinical research programs, ensuring process consistency, alignment, and compliance while resolving issues throughout the project lifecycle.
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Local Contact Person for Pharmacovigilance and Regulatory Affairs
Ergomed
Taipei, tw
25d
Local Country Person Responsible for Pharmacovigilance and Regulatory Affairs ensuring compliance with national requirements in Australia.
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PV Scientist
Biibhr
Maidenhead, United Kingdom
26d
Perform signal management activities and author comprehensive safety evaluations to ensure product safety and efficacy.
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Vice President and Global Head of Drug Safety and Pharmacovigilance
↗
Insmed Incorporated
Remote
$365k–$497k
26d
Lead global drug safety and pharmacovigilance (PV) strategy, operations, and compliance to ensure patient safety for rare disease treatments.
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Director/Head, Pharmacovigilance
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Orca Bio
Remote, US
26d
Lead the safety function and risk management for next-generation cell therapies treating blood cancer, ensuring regulatory compliance and patient safety.
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Director, Global Patient Safety Sciences Delivery - General Medicine
Regeneron
Dublin
$120k–$120k
26d
Lead global patient safety sciences delivery operations for General Medicine, ensuring high-quality, compliant execution of safety surveillance, signal management, and aggregate reporting.
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Lead Medical Project Coordinator
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Thermo Fisher Scientific
Desde casa, CO
27d
Lead coordination and oversight of medical projects, ensuring high-quality delivery and successful execution throughout the study lifecycle for clinical research.
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Safety Associate
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Iqvia
Remote
27d
Review, assess, and process safety data and information across service lines, distributing reports to internal and external third parties per regulations and SOPs.
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(Senior) Director, Drug Safety and Pharmacovigilance Operations
AbCellera
Vancouver
$160k–$160k
27d
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
Veeva
Remote
27d
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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Medical Director/Senior Medical Director - Nephrology (FSP)
Thermofisher
Remote, Argentina
28d
Provide medical oversight of clinical trials and marketed products, ensuring adherence to regulations and client directives while managing safety data and therapeutic expertise.
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Director, Global Patient Safety Sciences Delivery - General Medicine
Regeneron
TARRYTOWN, US
$205k–$205k
28d
Lead global patient safety sciences delivery operations for General Medicine, ensuring high-quality, compliant execution of safety surveillance, signal management, and aggregate reporting.
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Medical Information Associate
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PrimeVigilance
Melbourne, VIC, AU
28d
Support the Medical Information team by handling initial adverse event and medical information inquiries from healthcare professionals, patients, and pharmaceutical clients.
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Director, Global Patient Safety Sciences Delivery - Rare Disease
Regeneron
TARRYTOWN, US
$205k–$205k
28d
Lead global patient safety sciences delivery operations for rare disease portfolios, ensuring compliant execution of safety surveillance, signal management, and aggregate reporting.
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Med Info Spec I - Nuclear Pharmacist
Thermofisher
Morrisville, North Carolina, USA
28d
Provides technical and medical information, manages adverse events and product complaints, and supports clinical trial inquiries for pharmaceutical and device products.
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Med Info Spec I - Nuclear Pharmacist
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Thermo Fisher Scientific
Morrisville, NC, US
28d
Provides technical and medical information, manages adverse events and product complaints, and supports clinical trial inquiries for pharmaceutical and device products.
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Sr. Scientist Pharmacovigilance Operations Oversight and Strategy
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Haleon
TS, IN
28d
Ensures patient safety by overseeing global pharmacovigilance case processing, vendor quality/compliance, and safety data reporting for Haleon consumer health products.
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Sr. Scientist Pharmacovigilance Operations Oversight and Strategy
Gsknch
India - Andra Pradesh - Hyderabad
28d
Ensures patient safety by overseeing global pharmacovigilance case processing, vendor quality/compliance, and safety data reporting for Haleon's consumer health products.
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Senior Medical Information Associate
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PrimeVigilance
Melbourne, VIC, AU
28d
Support the Medical Information team by handling initial adverse event and medical information inquiries from external customers, including call handling.
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Associate Medical Information Manager
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PrimeVigilance
Melbourne, VIC, AU
28d
Line management of a Medical Information Team to deliver high-quality Medical Communications services and support global MI programs.
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Director - Safety Strategy
Veeva
China - Shanghai
28d
Lead the expansion of Veeva's Safety business in China, acting as a strategic advisor to modernize Pharmacovigilance operations through a unified cloud platform.
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Head of Multiple Myeloma & AML, Oncology - Global Patient Safety
AbbVie
North Chicago, IL, us
28d
Leading global patient safety and pharmacovigilance strategies for oncology products (Multiple Myeloma & AML) across the product lifecycle.
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Pharmacovigilance Senior Specialist
AbbVie
Bogota Cundinamarca, co
28d
Execute, coordinate, and monitor pharmacovigilance activities for North LATAM Cluster countries, serving as a functional liaison between internal teams, vendors, and business partners to ensure compliance with regulatory requirements and quality standards.
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Clinical Medical Monitor
Praxisprecisionmedicines
Remote
$260k–$260k
28d
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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Senior Medical Director, Immunology, Global Patient Safety
AbbVie
North Chicago, IL, us
28d
Lead patient safety strategy for immunology products across the lifecycle, managing pharmacovigilance, signal detection, and risk mitigation.
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Scientist/Senior Scientist – QPPV Office, Local Safety Support & Regulatory Intelligence
ClinChoice
Philippines - Pasig
29d
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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Pharmacovigilance Associate Scientist II
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Novotech
AU
29d
Conduct pharmacovigilance work including case processing, safety reporting, and project management for clinical trials.
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Manager, Safety Scientist
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Beone Medicines
Remote, US
$128k–$128k
29d
Conduct signal detection, evaluate safety data, assess risks, and manage regulatory reporting for pharmaceutical compounds.
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PV Scientist Quality Document Manager
Biibhr
Maidenhead, United Kingdom
29d
Manage quality of pharmacovigilance documents (Safety Surveillance and Aggregate reports) authored by internal teams and vendors to ensure data accuracy, stylistic consistency, and compliance with Biogen standards.
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Senior Medical Monitor
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Novotech
AU
29d
Provide medical oversight for clinical trials, develop monitoring plans, and review protocols and safety data for Novotech-sponsored studies.
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SERM/Safety Evaluation & Risk Management Physician
Gsk
Japan - Tokyo - Akasaka
1mo
Responsible for continuous safety assessment, risk management, and medical review of GSK Japan products in clinical development and post-marketing settings to ensure patient safety.
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Associate Director, Pharmacovigilance QA
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Novartis
Barcelona, CT, ES
$69k–$128k
1mo
Lead quality oversight and compliance for global Pharmacovigilance and Device Vigilance activities to ensure patient safety and regulatory alignment.
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Drug Safety Specialist (Night Shift)
Thermofisher
Remote, Philippines
1mo
Perform day-to-day Pharmacovigilance (PV) activities including data entry, coding, assessment of adverse events, case review, follow-up, tracking, and regulatory reporting to ensure patient safety.
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Drug Safety Specialist (Night Shift)
Thermofisher
Remote, Philippines
1mo
Perform day-to-day Pharmacovigilance (PV) activities including data entry, coding, assessment of adverse events, case review, follow-up, tracking, and regulatory reporting to ensure patient safety.
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Drug Safety Specialist (FSP) - Day Shift
Thermofisher
Remote, Philippines
1mo
Perform day-to-day Pharmacovigilance (PV) activities including data entry, coding, assessment of adverse events, case review, follow-up, tracking, and regulatory reporting to ensure patient safety.
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Senior Medical Project Coordinator
Thermofisher
Remote, Philippines
1mo
Manage, coordinate, and evaluate medical projects for clinical trials, ensuring process consistency, compliance, and optimal performance while representing the company in the medical research community.
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Senior/Principal Drug Safety Specialist (Night Shift)
Thermofisher
Remote, Philippines
1mo
Perform and oversee day-to-day Pharmacovigilance (PV) activities including collection, monitoring, assessment, evaluation, research, and tracking of safety information in a highly regulated environment.
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FSP Pharmacovigilance Coordinator
Thermofisher
Remote, Philippines
1mo
Coordinate project logistics, safety documentation, and data management for global and domestic clinical trials, focusing on adverse events and Data Safety Monitoring Boards.
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International PV Senior Specialist
Vrtx
Remote
$103k–$103k
1mo
Supports build-out and management of the global Pharmacovigilance (PV) structure, ensuring compliance with regulatory requirements and overseeing local Responsible Persons for Pharmacovigilance (RPPVs).
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Executive Director, Pharmacovigilance Systems & Enablement
Regeneron
Cambridge, MA, US
$255k–$255k
1mo
Executive Director leading PV systems strategy, data architecture, and AI-enabled capabilities for Global Patient Safety in a GxP environment.
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Qualified Person - PV, EU
Thermofisher
Remote, Bulgaria
1mo
Serves as the European Union (EU) and/or UK Qualified Person for Pharmacovigilance (QPPV) or Deputy QPPV for selected clients, ensuring regulatory compliance and overseeing drug safety services.
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Clinical Safety Analyst
AbbVie
Minato-ku, 13, jp
1mo
Evaluates and ensures the quality of clinical trial patient safety data through timely review, analysis, and reporting to support global safety surveillance.
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Safety Operations Intern-DL 2027
Iqvia
Remote
1mo
Assist managers in processing adverse drug reaction safety data, including collecting and tracking adverse events (AE) and endpoint information, managing project workflows, database entry, quality control, and preparing safety submission dossiers.
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(Senior) Medical Director - Rheumatology, EMEA (Client - Dedicated)
Thermofisher
Remote, Sweden
1mo
Provide medical leadership and support for clinical trials and safety evaluation within the Pharmacovigilance department, ensuring medical validity of study endpoints and subject safety.
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(Senior) Medical Director - Dermatology/ Allergology/ Immunology, EMEA (Client-Dedicated)
Thermofisher
Remote, Portugal
1mo
Provide medical leadership and safety evaluation for Dermatology clinical trials within the PPD Pharmacovigilance department.
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Medical Information Pharmacist Manager
Thermofisher
Morrisville, North Carolina, USA
1mo
Lead a small team of Medical Information professionals while functioning as a practicing Medical Information Pharmacist to manage pharmaceutical operations, ensure quality compliance for clinical trials, and handle complex medical inquiries.
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Senior Medical Director - Patient Safety
AbbVie
South San Francisco, CA, us
1mo
Lead patient safety strategy for late-stage oncology products, managing surveillance, signal detection, and risk management from pre-clinical through NDA submission.
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Senior Specialist, Regulatory & PV Network
Ergomed
Sofia, Sofia City Province, bg
1mo
Develop regulatory strategy and drive PV deliverables for pharmaceutical clients, acting as the local Pharmacovigilance contact person.
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