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Name
Cathy Carfagno
Title
Principle, Surf the Line Consulting LLC
Bio
Ms. Carfagno is an authority on the business processes and associated use of information technology in the end-to-end drug development process with a focus on clinical and regulatory.
Over multiple decades working in various organizations such as Merck & Co., Merck J&J Joint Venture, IMS and Prudential, both in business and IT roles she was recognized for her leadership and represented these organizations on multiple internal transformational teams and industry initiatives.
Now consulting, she is following the continuing technology Innovation adoption storyline. Dedicated to partnering with the many voices in the drug development process to continually progress towards innovation and efficiency as they surf the tech line and catch the next innovation wave and investment opportunity.
She has been a speaker/consultant at various forums:
• Chairman Industry Clinical Portal Forum
• TransCelerate Bio Pharma
• DIA Regulatory Submissions, Information, and Document Management Forum
• SCOPE Summit for Clinical Ops Executives
• Industry of Things World USA
Education: BA Business Administration; Master of Science, Masters Certificate in Technical Leadership
Specialties: Clinical Trial Management, Account, Budget, Contract and Portfolio Management
Certified: Project Management Professional (PMP), Six Sigma Green Belt (SSCGB), Change Agent Capabilities (CAC), Scrum Master (CSM)
Over multiple decades working in various organizations such as Merck & Co., Merck J&J Joint Venture, IMS and Prudential, both in business and IT roles she was recognized for her leadership and represented these organizations on multiple internal transformational teams and industry initiatives.
Now consulting, she is following the continuing technology Innovation adoption storyline. Dedicated to partnering with the many voices in the drug development process to continually progress towards innovation and efficiency as they surf the tech line and catch the next innovation wave and investment opportunity.
She has been a speaker/consultant at various forums:
• Chairman Industry Clinical Portal Forum
• TransCelerate Bio Pharma
• DIA Regulatory Submissions, Information, and Document Management Forum
• SCOPE Summit for Clinical Ops Executives
• Industry of Things World USA
Education: BA Business Administration; Master of Science, Masters Certificate in Technical Leadership
Specialties: Clinical Trial Management, Account, Budget, Contract and Portfolio Management
Certified: Project Management Professional (PMP), Six Sigma Green Belt (SSCGB), Change Agent Capabilities (CAC), Scrum Master (CSM)
