Pharmacovigilance Jobs in Newark
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Search Results - Pharmacovigilance Jobs in Newark
Daiichi Sankyo, Inc.-Newark
vendor outsourcing agreements, PV Agreements (PVAs) and Safety Data Exchange Agreements (SDEAs). Maintains oversight of DSI contracts that are PV relevant and AE reporting language in associated contractual templates. Ensures Good Pharmacovigilance...
New York, 9 mi from Newark
Director, Pharmacovigilance (PV) Clinical Trials Operations
at ClinChoice (View all jobs)
United States
Location: United States - Homebased
Schedule: Permanent- FTE
ClinChoice is a global full-service CRO dedicated to professional development...
pharmiweb.jobs -
Daiichi Sankyo, Inc.-Newark
GPT) as an ad hoc member and independently provides strategic and operational leadership on new product labeling in collaboration with the Global Regulatory Leads (GRLs) and Clinical Safety & Pharmacovigilance (CSPV) for assigned products.
This position...
ECLARO-Lawrenceville (NJ), 42 mi from Newark
Pharmacovigilance Specialist
Job Number: (phone number removed)
Be part of a company that delivers life-changing healthcare solutions. ECLARO is looking for a Pharmacovigilance Specialist for our client in Lawrenceville, NJ.
ECLARO’s client...
resume-library.com -
Daiichi Sankyo, Inc.-Newark
Development, Biostatistics and Data Management, Regulatory Affairs, Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance, Regulatory/Risk Management, Quality Assurance, Medical Affairs, Translational Research, Research, Informatics...
SpringWorks Therapeutics, Inc.-Stamford, 40 mi from Newark
Your Role:
The Global Pharmacovigilance Medical Director will lead a variety of core medical activities within the safety organization to support the monitoring and evaluation of the safety profile of assigned products. This individual...
appcast.io -
The Fountain Group LLC-Clark (NJ), 11 mi from Newark
exploitation experience in pharmacovigilance.
• Minimum of 3-5 years of relevant experience.
• Experience in MedDRA coding preferred.
• Basic understanding of US Regulations pertaining to Post Marketing Safety preferred.
• Knowledge of medical terminology...
resume-library.com -
Binding Minds Inc. (Certified Disability Owned Business Enterprise)-Basking Ridge, 20 mi from Newark
for changes to processes.
Supports the maintenance of all documentation files, including forms and templates, and communicates updates/revisions to documents.
Experience Qualifications
3 or more years of Pharmacovigilance experience in a pharmaceutical...
mindmatch.ai -
HireTalent-Basking Ridge, 20 mi from Newark
/revisions to documents.
Experience Qualifications
3 or more years of Pharmacovigilance experience in a pharmaceutical, biotechnology or related environment preferred
Possesses knowledge of Food and Drug Administration (FDA) regulations, European Union...
resume-library.com -
GForce Life Sciences-Clark (NJ), 11 mi from Newark
or a related field preferred.
• 3–5 years of relevant experience in case processing or pharmacovigilance.
• Familiarity with MedDRA coding and U.S. Post-Marketing Safety regulations is a plus.
• Strong organizational skills, attention to detail, and the ability...
mindmatch.ai -
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