Cecily Johnson

Senior Director / Business Unit Lead, Medical Devices & Innovative Products at PrimeVigilance

Cecily Johnson is a seasoned professional in the field of medical device and innovative products, currently serving as Senior Director and Business Unit Lead at PrimeVigilance since August 2020. Johnson has held various leadership roles in project and safety data management within PrimeVigilance, including Director of Projects and Director of Safety Data Management. Prior to this, Johnson was associated with Ashfield, part of UDG Healthcare plc, as Associate Director of PV Operations, and also served as Operations Manager. Johnson’s earlier experience includes positions at IQVIA, where roles ranged from Quality Manager to Operations Specialist Associate Manager, and at PPD focusing on safety coordination. Johnson began the career at Labcorp as a Technologist Customer Service Representative. Educationally, Johnson holds a Bachelor of Science degree in Biology and Sociology from the University of North Carolina at Chapel Hill.

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Raleigh, United States

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PrimeVigilance

PrimeVigilance, an Ergomed company, was set up by former Pharmacovigilance Regulators in 2008. We have grown to become the leading Pharmacovigilance specialist company, delivering global solutions for both clinical safety and post-marketing pharmacovigilance, as well as medical information from our offices. Having successfully delivered Pharmacovigilance (PV) and Medical Information (MI) services for over 14 years, our experience enables us to offer a comprehensive, top quality, cost-effective, and innovative safety solution. Our flexible approach, tailor-made to work with clients, allows us to deliver the services that meet your clinical and post-marketing needs. From its operational hubs based in Europe, the USA, and Japan. PrimeVigilance manages a global Pharmacovigilance system with a choice of leading drug safety databases, stretching to more than 100 countries. • 900+ highly qualified professionals • Global leader in QPPV services • 24/7 multilingual call center • Choice of leading drug safety databases • Robotic Process Automation (RPA) expertise • Access to regulatory experts and key opinion leaders GLOBAL LIFE CYCLE MANAGEMENT SERVICES • PHARMACOVIGILANCE • PHARMACOEPIDEMIOLOGY & BENEFIT-RISK MANAGEMENT • AUDIT & INSPECTION • QUALITY MANAGEMENT • REGULATORY SCIENCE


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501-1,000

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