Patient Recruitment Videos

  1. Hosting Patient Engagement Networks To Hear The Patient Voice 4/24/2020

    In February 2020 Clinical Leader Live presented a virtual conference on the topic of patient centricity. The goal of the first session was to discover what pharma companies were doing to hear the voice of patients. In this video, Helen Kellar-Wood, Immunoscience Lead, Diversity & Patient Engagement, Bristol-Myers Squibb, discusses how the company uses patient engagement networks (PENs) to understand the patient journey.

  2. ClinCard Rideshare Integration With Lyft: A Site Success Story 9/19/2019

    Director of Clinical Research at MidLantic Urology, Cheryl Zinar, discusses how introducing rideshare has improved the clinical trial experience for all stakeholders – Added convenience and removed out-of-pocket costs for patients, simple workflow and improved control for study coordinators and increased enrollment and reduced costs for the site.

  3. Real Patient Stories: The Trials Of Finding Clinical Trials Online 2/26/2019

    For sponsors, it can be frustrating trying to recruit participants for clinical trials. For patients, trying to find a clinical trial can be equally frustrating. See patients and caregivers reactions when they are shown the easy to understand and navigate website powered by TrialScope Engage.

  4. How eConsent Improves Consent Development 11/1/2016

    Developing informed consent content requires a lot of back and forth communication between multiple stakeholders - an inefficient, slow process with a history of allowing unapproved or out-of-date consents to be accidentally deployed to sites. Electronic Informed Consent (eConsent) offers a streamlined, collaborative process that promotes faster content development, approval and deployment on one platform, guaranteeing that only the most current and approved consent version is used each time.

  5. The Value Of Electronic Informed Consent 11/1/2016

    Securing informed consent from clinical trial participants involves more than a signature—you need to ensure participants truly understand what they’re signing.  Learn from industry expert, Sandra “SAM” Sather, on how the electronic informed consent (eConsent) process improves the way participants are consented on a clinical trial.

  6. Reducing Regulatory Risk In Clinical Trials With eConsent 11/1/2016

    You may already know too well the challenges of a paper-based Informed Consent process, but did you know that Informed Consent is one of the most cited deficiencies by regulatory authorities? Paper-based informed consent increases your risk for delayed approvals, fines, litigation and even trial failure.

  7. 3 Major Regulatory Risks You Can Reduce With Electronic Informed Consent 11/1/2016

    You may already know too well the challenges of a paper-based Informed Consent process, but did you know that Informed Consent is one of the most cited deficiencies by regulatory authorities? Paper-based informed consent increases your risk for delayed approvals, fines, litigation and even trial failure.

  8. Recruiting And Retaining Patients With eConsent 11/1/2016

    The informed consent process intends to ensure trial participants understand the risks and benefits of joining your trial, but a poor experience leads to low recruitment rates and costly drop-outs. Electronic Informed Consent (eConsent) improves recruitment and retention of participants by developing better comprehension of consent materials and improving engagement for the full duration of your study. In this short video, industry expert Sandra "Sam" Sather, reviews the ways that eConsent supports and adds value to the recruitment process.