Sandra "SAM" Sather

Sandra “SAM” Sather, MS, BSN, CCRA, CCRC, 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. She 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. SAM has held clinical research industry certifications for over 15 years by the Association for Clinical Research Professionals (ACRP). She is a current member of the ACRP Academy Board of Trustees, and Regulatory Affairs Committee (RAC). SAM is a frequent subject matter expert for GCP regulation and speaker at industry conferences. Sam has authored many competency-based curriculums for various clinical research stakeholders.

  • Monitoring Considerations for Clinical Trials with eConsent1:01:36

    Monitoring Considerations for Clinical Trials with eConsent

    During this webinar, informed consent experts with decades of hands-on monitoring experience discuss the challenges they’ve encountered and how to overcome them with the integration of eConsent.

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  • Tips for Implementing an eConsent Solution3:05

    Tips for Implementing an eConsent Solution

    Industry expert Sandra "SAM" Sather shares her knowledge of how to properly implement an eConsent solution.

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  • Preparing for eConsent - A Step by Step Guide for Site Personnel

    Preparing for eConsent - A Step by Step Guide for Site Personnel

    5 steps to help sites prepare for implementing an electronic informed consent (eConsent) solution.

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  • FDA Supports Innovation in Clinical Trials with eConsent4:12

    FDA Supports Innovation in Clinical Trials with eConsent

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  • Visibility and Oversight: What Paper Informed Consent Isn't Offering You58:03

    Visibility and Oversight: What Paper Informed Consent Isn't Offering You

    Speakers from Chesapeake IRB and CRF Health discuss informed consent oversight and visibility. See how electronic informed consent (eConsent) enables top pharma companies achieve greater transparency.

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  • 3 Major Regulatory Risks You Can Reduce with Electronic Informed Consent54:25

    3 Major Regulatory Risks You Can Reduce with Electronic Informed Consent

    Does your clinical trial’s informed consent process stand up under regulatory scrutiny? Learn how eConsent can help to mitigate such risks as approval delay, fines, litigation, even trial failure.

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  • Innovations in e-Consent: Reducing Regulatory Risk While Improving Participant Comprehension1:00:01

    Innovations in e-Consent: Reducing Regulatory Risk While Improving Participant Comprehension

    As regulatory agencies push for more effective informed consent processes in clinical trials, eConsent can mitigate regulatory risk, while improving patient comprehension, compliance, and retention.

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