Get to Know the Presenters for CRF Health's Upcoming Webinar: Electronic Informed Consent: 2017 Industry Survey Results from Clinical Sites
Sam Sather, Quality and Regulatory, TrialConsent, CRF Health
Sam's current focus of consulting is to promote clinical quality systems for Sponsors/CROs, Investigators and clinical research institutions. She has over 30 years of clinical experience, a Bachelor of Science degree in Nursing and a Master of Science degree in Education with a Specialization in Training and Performance Improvement.
Sam has served many roles in clinical research, including site study coordinator and manager, sponsor and CRO monitor, quality assurance auditor, risk manager, trainer, and performance management consultant. She has held clinical research industry certifications for over 15 years by the Association of Clinical Research Professionals (ACRP). Sam is a current member of the ACRP Academy Board of Trustees, and Regulatory Affairs Committee (RAC). She is a frequent subject matter expert for GCP regulation and a speaker at industry conferences. Sam has authored dozens of competency based curriculums for various clinical research stakeholders.
Giga Smith, Director of Research, Coastal Carolina Health Care
Giga Smith is the Director of Research for Coastal Carolina Health Care and Research, a large multi specialty, private practice and research site in New Bern, NC, where she was responsible for starting their research program in 2015.
Giga has worked in clinical research since 1991 in roles such as study coordinator, project manager for CROs and pharmaceutical sponsors, and business development for CROs and patient recruitment providers.
As the executive Director of Research at Greenway Health, Giga managed studies and sites that utilized technologies to facilitate direct data entry into EDC systems.
Title: Electronic Informed Consent: 2017 Industry Survey Results from Clinical Sites
When: October 10, 2017 | 11:00 a.m. - 12 p.m. EDT (hosted by Xtalks)
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