Judy Gibson, CCRC
clinical research professional | quality assurance | data management | technology solutions@ Suvoda
Atlanta, Georgia, United States
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Judy Gibson, CCRC is a highly experienced self-starter with 14 years in the healthcare industry, specializing in Phase I-IV clinical research trials. She has a strong understanding of FDA regulations and submission requirements, as well as experience in EMR systems and sponsoring dedicated IVRS and EDC systems. Judy is responsible for preparing regulatory submissions and maintaining the Trial Master File. She is organized, detail-oriented, and has successfully led various team projects with strict deadlines.
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Emails and Phone Numbers

@verily.com
@gmail.com
@signalpath.com
@signalpath.com
@verily.com
@suvoda.com
+1 610572****
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About

*Motivated self-starter with 14 years in the healthcare industry, 10 years of experience focused on conducting Phase I-IV clinical research trials in Oncology, Gastroenterology, Urology, and Neurology in a direct client and vendor-facing role *Understanding of FDA regulations, guidance, and submission requirements *Experienced in various EMR systems and sponsor dedicated IVRS and EDC systems, including Medidata Rave, Oracle, Inform, Nexttrials Prism, TAO, etc. *Responsible for the preparation of Regulatory submissions and maintenance of the Trial Master File *Responsible for participate recruitment and retention, as well as, proper education of investigational products, procedures, and trial requirements for potential volunteers *Organized and detail-oriented team member successfully leading various team projects with strict deadlines

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Work Experience

6 Tower Bridge, Conshohocken, PA, 19428, US

Pharmaceutical Manufacturing

821
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Judy Gibson, CCRC's Professional Milestones

  • Clinical Trial Protocol Digitizer / Quality Assessment (2017-05-01~2018-08-01): Delivered accurate and comprehensive medication treatment plans, ensuring the safety and security of patients.
  • Clinical Research COOrdinator (2015-07-01~2017-12-01): Coordinated successful clinical trials, delivering successful outcomes for patients.
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