Pharmacovigilance Jobs in North Carolina
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Search Results - Pharmacovigilance Jobs in North Carolina
Thermo Fisher ScientificCharlotte
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
FSP Associate Manager, Safety Data and Systems - Pharmacovigilance
• Design, develop and validate AI/ML and NLP components that support safety operations...
Aptino, Inc.Cary
We're Hiring: Pharmacovigilance Coordinator
📍 Location: Cary, NC 27513 (Remote after initial 2 weeks onsite training)
⏳ Duration: 6 Months
🕒 Schedule: Monday–Friday, 9 AM–6 PM EST or 10 AM–7 PM EST
Work Arrangement:
Candidates must live...
Thermo Fisher ScientificRaleigh
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
FSP Associate Manager, Safety Data and Systems - Pharmacovigilance
• Design, develop and validate AI/ML and NLP components that support safety operations...
Amerit ConsultingCary
OVERVIEW:
Our client, a Global Fortune 50 organization and one of world’s largest distributors of Health care systems, medical supplies & Pharmaceutical products, seeks an accomplished “Pharmacovigilance Reporting Specialist”
** JOB ID: JP00007260...
Thermo Fisher ScientificGreensboro
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
FSP Associate Manager, Safety Data and Systems - Pharmacovigilance
• Design, develop and validate AI/ML and NLP components that support safety operations...
KaztronixDurhamappcast.io
data integrity, and guiding medical decisions across development programs.
The ideal candidate will lead safety reviews, interpret virologic and liver-function data, collaborate with Clinical Operations, Pharmacovigilance, Regulatory Affairs, and
#J...
Thermo Fisher ScientificChapel Hill (NC)
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Join Us as a Associate Director, PV
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our...
KaztronixDurhamappcast.io
Pharmacovigilance, Regulatory Affairs, and external investigators to support the safe and effective execution of clinical studies. The ideal candidate will bring strong experience in medical monitoring, clinical trial oversight, safety review, and the interpretation...
AdeccoCaryadecco.com
and pharmacovigilance activities.
If you have experience in a pharmacy, oncology, clinical, or healthcare setting and thrive in a fast-paced environment where accuracy matters, this could be the perfect opportunity for you!
• Location: Must reside within 60 miles...
Milestone Technologies, Inc.Charlotte
/satisfaction and program effectiveness.
• Identify and report pharmacovigilance information as required (Adverse Events, Product Quality Complaints, etc.)
Required Qualifications
• Bachelor’s degree required (preferably in a health, scientific, or business...
Avery Healthcare Group Ltd.Durham
across regulatory, clinical operations, supply, real world evidence, pharmacovigilance, commercial, and medical stakeholders is preferred.
• Prior experience within a managed access provider, CRO, pharmaceutical company, biotechnology company...
AerogenCharlotteappcast.io
and actionable insights.
• Partner cross-functionally with Clinical Operations, Regulatory Affairs, Pharmacovigilance, Commercial, Market Access, and R&D to deliver product-driven initiatives and ensure consistent medical messaging.
• Provide medical input...
IQVIADurhamappcast.io
Attends and presents at Investigator Meetings. - May perform medical case review of Serious Adverse Events (SAEs), including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department. - May provide medical...
5PY IQVIA RDS Inc.Durhamappcast.io
in collaboration with the Pharmacovigilance department.
• May provide medical support for the Analysis of Similar Events (AOSE), in collaboration with or on behalf of Pharmacovigilance department.
• May perform medical review of adverse event coding.
• Performs...
Aerogen Ltd.Raleighappcast.io
review of emerging safety and efficacy data, identification and escalation of potential trends or signals, and assessment of evolving benefit–risk, in close collaboration with Pharmacovigilance.
• Serve as the clinical subject-matter expert for assigned...
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