Senior Associate, Pharmacovigilance - US - Remote
Worldwide Clinical Trials(3 months ago)
About this role
Senior Pharmacovigilance role at a global CRO focused on ensuring drug safety during pre-approval clinical trials. The position supports the safety lifecycle of investigational products and works with internal and external stakeholders to maintain regulatory compliance and quality standards.
Required Skills
- Pharmacovigilance
- SAE Review
- Safety Database
- Regulatory Submissions
- Safety Reporting
- Data Entry
- Quality Control
- Medical Terminology
- Database Management
- Communication
+2 more
Qualifications
- Bachelor's Degree in Science
- Nursing Degree
About Worldwide Clinical Trials
worldwide.comWorldwide Clinical Trials is a top-rated, full-service global CRO. We provide 30+ years of clinical expertise to benefit your study. Learn more about us here.
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