Carrie Senter
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Executive Summary
Carrie Senter is a highly experienced Clinical Research, Pharmacovigilance, and Regulatory Affairs professional with over 30 years of expertise in drug and device development. She has worked on Phase I-IV and post-approval projects, including Phase I-IV and post-approval projects. Carrie is skilled in ARGUS and ArisG Safety Database systems and has experience in regulatory submissions related to IND, NDA, IDE, and BLA regulated product development. She is proficient in vendor management, contract negotiation, SDEA development, and maintenance. Carrie is a results-oriented manager with excellent process development and team leadership skills.
Contact Information
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PrimeVigilance
director of projects at primevigilance ltd
director of projects at primevigilance ltd
Professional Background
Personal Interests
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