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.

  • 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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  • In Pursuit of eConsent: Best Practice Recommendations for Successful Integration

    In Pursuit of eConsent: Best Practice Recommendations for Successful Integration

    Provided by The Journal for Clinical Studies - Original at https://issuu.com/mark123/docs/jcs_volume_9_2_web/58 For more information about electronic informed consent please visit www.crfhealth.com

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  • Using eConsent in Clinical Research to Support Patient Understanding and Welfare

    Using eConsent in Clinical Research to Support Patient Understanding and Welfare

    Deciding to participate in a clinical trial is not risk-free for anyone. This article explores how to best support patients during the informed consent process (ICP) with eConsent.

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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.

    Watch Video
  • 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.

    Watch Video
  • 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.

    Watch Video
  • Electronic Informed Consent: 2017 Industry Survey Results55:21

    Electronic Informed Consent: 2017 Industry Survey Results

    Sam Sather, Regulatory & Quality Lead for TrialConsent™, discusses survey findings from the State of eConsent 2017 Report. Find out why 82% of pharma companies are projected to adopt eConsent by 2020.

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  • Electronic Informed Consent - 2017 Industry Survey Results from Clinical Sites1:02:32

    Electronic Informed Consent - 2017 Industry Survey Results from Clinical Sites

    In this webinar, CRF Health's Sandra "SAM" Sather is joined by Giga Smith from Coastal Carolina Healthcare (CCHC) to discuss Electronic Informed Consent (eConsent) from the research site perspective.

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  • 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.

    Watch Video
  • 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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  • 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.

    Watch Video
  • 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.

    Read Article
  • Translations and eConsent3:13

    Translations and eConsent

    When designing an informed consent, it's extremely important to consider the participants using it. Specifically, the consent should be created in a language that its primary audience will understand.

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  • Can Seniors Use eConsent?2:45

    Can Seniors Use eConsent?

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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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  • FDA Supports Innovation in Clinical Trials with eConsent4:12

    FDA Supports Innovation in Clinical Trials with eConsent

    Watch Video
  • 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.

    Watch Video
  • 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.

    Watch Video
  • 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.

    Watch Video
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