Cassandra Chando
Regulatory Submissions Manager@ Medpace
Raleigh, North Carolina, United States
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Cassandra Chando is a highly experienced professional with 13.9 years of work experience in the pharmaceutical industry. She has a strong background in clinical trials, good clinical practice, and clinical research. Currently, she holds the position of Global Regulatory and Startup Lead at QuintilesIMS. Throughout her career, she has worked in various roles, including Regulatory Submissions Manager at Medpace, Site Activation Manager at IQVIA, and Senior Clinical Trial Specialist at Parexel. Cassandra's expertise lies in standard operating procedures and oncology. She is based in the United States.
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Emails and Phone Numbers

@medpace.com
@iqvia.com
@parexel.com
+1 513579****
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About

Global Regulatory and Startup Lead at QuintilesIMS

Work Experience

5375 Medpace Way, Cincinnati, OH, 45227, US

Pharmaceutical Manufacturing

5169
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Cassandra Chando's Professional Milestones

  • Site Activation Manager (2014-01-01~): Successfully managed and executed major program launches, meeting the deadlines and objectives for a successful site activation.
  • Senior Startup Specialist (2009-11-01~2011-05-01): Successfully launched multiple startups, driving company growth and expanding market reach.
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Education

North Carolina State University
North Carolina State University

Psychology,

Bachelors

2004-2008