16 pharmacovigilance specialist jobs at 11 companies in United States
2w
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Pharmacovigilance Specialist
United States
OnsiteFull Time
1+ YOEMinimum 1 year pharmacovigilance experience, case assessment and safety case processing experience, Argus/Argus J proficiency, J-Assessments and PMDA reporting knowledge, Japanese (native or JLPT N1) and business-level English.
Argus, Argus J, ICSR Creation Tool
2w
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Pharmacovigilance Specialist
United States
OnsiteFull Time
1+ YOE1+ year pharmacovigilance or case assessment experience, Argus/Argus J experience, ability to perform J-Assessments and PMDA reporting, Japanese native or JLPT N1, business-level English, bachelor's or healthcare degree or nursing qualification.
Argus, Argus J, ICSR Creation Tool
1mo
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Pharmacovigilance Specialist - US - Remote
Durham or Brasilia or United Kingdom or Mexico City or Belgrade
$50k-$99k/yr RemoteFull Time
1+ YOEBachelor's in science or nursing, minimum 1 year pharmacovigilance experience, EMR/safety database and MS Office proficiency, strong medical terminology and communication skills, English fluency.
MS Office, Microsoft Excel, Microsoft PowerPoint, Microsoft Word
1mo
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Specialist, Pharmacovigilance
Pittsburgh, Pennsylvania, United States
$19-$26/hr OnsiteFull Time
2+ YOE2+ years healthcare/pharmacy experience preferred; associate degree or equivalent experience; proficiency with Microsoft Word, PowerPoint, SharePoint, Excel; strong communication and quality/QA skills.
Microsoft Word, Microsoft PowerPoint, Microsoft SharePoint, Microsoft Excel
2w
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Pharmacovigilance Specialist
United States
OnsiteFull Time
1+ YOEProcess and assess safety cases in Argus/Argus J, perform J-Assessments and PMDA reporting, generate PMDA XML, apply product labeling, and maintain regulatory compliance.
Argus, Argus J, ICSR Creation Tool
2w
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Pharmacovigilance Specialist
United States
OnsiteFull Time
1+ YOEMinimum 1 year PV case assessment/safety case processing experience, experience with Argus/Argus J, J-Assessments and PMDA reporting, Japanese (native or JLPT N1) and business-level English, bachelor's degree or equivalent clinical qualification.
Argus, Argus J, ICSR Creation Tool
2w
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Principal Pharmacovigilance Specialist, Case Processing
Raleigh or United States
RemoteFull Time
4+ YOEBachelor's degree in life sciences and four years of related experience required. Requires advanced pharmacovigilance knowledge, safety database experience, communication, project management, accuracy, and problem-solving skills.
Oracle Argus Safety, ARISg
1d
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Senior Post-Market Pharmacovigilance Specialist (Remote)
United States
RemoteFull Time
5+ YOERequires 5+ years in drug safety or pharmacovigilance, scientific or medical expertise, safety database experience, MedDRA and WHO drug dictionary coding, regulatory knowledge, and project leadership skills.
ICH E2A, ICH E2B(R3), ICH E2D, MedDRA, WHO drug dictionary, Microsoft Office, ISO 9001, ISO 27001, 21 CFR Part 11, FDA, GCP
2d
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Pharmacovigilance QA Auditor Specialist
Raritan or Horsham or Titusville
$79k-$128k/yr HybridFull Time
4+ YOEBachelor’s degree required, preferably in life, natural, or computer science; 4+ years of pharmacovigilance experience, project management, auditing, data analysis, communication, and Microsoft Office proficiency.
Microsoft Outlook, Microsoft PowerPoint, Microsoft Excel, Microsoft Word
2d
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Pharmacovigilance QA Auditor Specialist
Raritan or Horsham or Titusville
$79k-$128k/yr HybridFull Time
4+ YOEBachelor’s degree required, 4+ years of pharmacovigilance experience, project management, auditing knowledge, data analysis, critical thinking, collaboration, presentation skills, and Microsoft Office proficiency.
Microsoft Outlook, Microsoft PowerPoint, Microsoft Excel, Microsoft Word, Agile
1mo
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Pharmacovigilance Specialist I, II, III
Columbus, Ohio, United States
$68k-$92k/yr HybridFull Time
1+ YOEBachelor's in healthcare-related field required; 1+ years adverse event reporting or regulated healthcare ops; knowledge of FDA AE/PC reporting, GDP/ALCOA, QMS systems; able to investigate patient-reported events and meet 24-hour reporting timelines.
2mo
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Senior Specialist I, Postmarketing Patient Safety and Pharmacovigilance Operations
Redwood City, California, United States
$104k-$137k/yr OnsiteFull Time
3+ YOE3+ years pharmacovigilance experience in a global/post-marketing environment; knowledge of Argus, MedDRA, WHO Drug coding, FDA/EU/ICH safety guidelines; experience with vendor oversight, quality review, SOPs, training, audits.
Argus, MedDRA, WHO Drug
2d
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PV Risk Management Specialist
Deerfield, Illinois, United States
$112k-$154k/yr OnsiteFull Time
2+ YOEBachelor’s degree in a relevant scientific or clinical field, 2+ years of pharmaceutical industry experience, 2–3 years authoring PV-RMPs, regulatory knowledge, technical writing, analytical, and project management skills.
2d
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PV Risk Management Specialist
Deerfield, Illinois, United States
$112k-$154k/yr OnsiteFull Time
2+ YOEBachelor’s degree in a relevant scientific or clinical field, 2+ years pharmaceutical industry experience, 2–3 years authoring PV-RMPs, regulatory knowledge, writing, analytical, and project management skills.
Pharmacovigilance Risk Management Plans (PV-RMPs), European Union Risk Management Plans (EU RMPs)
3w
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Safety Surveillance Support Specialist
Fort Detrick, Maryland, United States
$85k-$95k/yr OnsiteFull Time
3+ YOEBachelor's in life sciences or related, 3+ years pharmacovigilance/drug safety, familiarity with Argus, knowledge of FDA and ICH reporting, able to process safety cases and regulatory submissions.
Argus, MedWatch
1mo
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VIE – Global Patient Safety Americas
Boston, Massachusetts, United States
OnsiteFull Time, Contract
Master's in life sciences or pharmacy, strong interest in pharmacovigilance/drug safety, fluent English, organized with stakeholder management skills; GVP knowledge is a plus.
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