August 17, 2021 (12:00 PM-1:00 PM ET)
Decentralized technology will change how sites, sponsors, and patients experience the study. How? Harnessing technology will increase the flexibility of protocol designs to expand patient access, accelerate operations, and reduce costs.
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September 21, 2021 (12:00 PM-1:00 PM ET)
Lack of diversity in clinical trials isn’t a new phenomenon for our industry. What actions can we take to improve diversity recruitment and retention to support the site? In this webinar, we will explore site-level strategies, building trust within the patient community, and leveraging data to identify gaps in our processes for continued community engagement.
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October 5, 2021 (10:00 AM-11:00 AM ET)
Scientific development has always been founded on the latest technology. Today, this means the explosion of digitalization of medical information. When it comes to drug development, the hurdle is access to the right patients, whether it be finding enough patients of different ethnicities, or finding enough patients with a specific confluence of phenotypic markers fitting a clinical trial protocol. Today, the digitalization of medical records has unleashed the possibility of searching for patients across institutions, enabling trial researchers to work with patients on a global scale. Trial protocols can be tested and modified against live patient data, sites with large clusters of eligible patients can be identified, and patients can be reidentified for trial recruitment at any site. In this webinar, we will outline the current trends, and offer real-world case studies.
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November 2, 2021 (12:00 PM-1:00 PM ET)
In this webinar, you’ll learn how the GTO team at Merck is using data and technology to reduce site burden related to oncology trial enrollment and visit management so that research staff can focus on their work with patients.
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November 9, 2021 (12:00 PM-1:00 PM ET)
This session is intended for sponsors and CROs to better understand the complexities of how research sites evaluate and value technology. Each site has different needs and challenges. We’ll bust the notion that one size fits all when it comes to research sites and technology.
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December 7, 2021 (12:00 PM-1:00 PM ET)
Recent global events have catalyzed the urgency around improving diversity, equity, and inclusion (DEI) in clinical research, but there is still much work to be done. Many conversations focus on race and ethnicity, while trial exclusivity must extend to age, gender identity, religion, and more. Recent discussions on DEI have been mostly US-centric instead of including other regions, all of which have their own DEI challenges. This global panel of experts will discuss the challenges to improve DEI and success strategies and pitfalls to avoid overcoming them.
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January 11, 2022 (12:00 PM-1:00 PM ET)
An in-depth qualitative research study. Sharing insights from rare disease patients and caregivers, focused on the patient perspective in clinical trial participation.
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January 18, 2022 (12:00 PM-1:00 PM ET)
ZS sponsored a multi-arm study to understand trial site team experiences, potential participant perceptions, and gaps in engagement of historically underrepresented patient communities. In this presentation, ZS will present results from the survey regarding sites and patients. Sanofi will present their approach to site and patient focused feasibility.
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February 22, 2022 (12:00 PM-1:30 PM ET)
Join us at this SCRS - Sanofi Symposium to celebrate/exemplify Patient centric approach and exchange on best practices from sites. Through the consideration of patient insights, sites and sponsors work tirelessly to produce healthcare solutions that are committed to enhanced patient experiences as well as an improved health-related quality of life. Efforts are increasing to ensure representation of inclusive and diverse populations in clinical trials while focusing on the continued development of consistent patient-centric strategies.
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March 15, 2022 (12:00 PM-1:30 PM ET)
With no existing site relationship, patients from third party referral companies can be unvetted and uninterested. This webinar presented by SubjectWell will explore what vendors can do for sites to make patient referrals more effective, including techniques that have been successfully utilized in other industries.
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April 19, 2022 (12:00 PM-1:00 PM ET)
According to the Tufts Center for the Study of Drug Development, the number of investigational drugs targeting cancer has nearly quadrupled since 2000, from 421 trials two decades ago to almost 1,500 trials in 2021. Life sciences companies focused on oncology are increasingly shifting toward precision medicine, but as they do so, it becomes harder to find clinical trial participants that fit the selective criteria. Additionally, once you do find participants, we also need to ensure you are retaining them.
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April 26, 2022 (12:00 PM-1:00 PM ET)
Research compliance professionals routinely confront complex and uncertain situations. Questions often arise about improving informed consent compliance, addressing weightier compliance risks throughout institutions, or increasing the chances a new compliance initiative might succeed. But the most challenging of compliance entanglements are all too often unexpected and imperceptible: research compliance professionals haven’t realized they should be paying attention, or why they need to. The reason? Blind spots. In this webinar, Draco Forte and David Staley of Advarra offer three strategies to check and reduce blind spots regularly to improve compliance oversight.
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May 24, 2022 (12:00 PM-1:00 PM ET)
Sites encounter a variety of challenges when navigating the complex clinical trial ecosystem, especially when it comes to implementing a multitude of technologies. In this webinar, discover how to do more with less while accelerating study start up with more efficient remote monitoring and RSDV. Complion Founder and CEO Rick Arlow will look at some of the lessons learned from top research sites and provide a framework for evaluating eReg/eISF systems. We’ll alsol discuss how your site can be awarded more studies by having the digital infrastructure required for remote studies and how to improve partner collaboration.
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June 7, 2022 (12:00 PM-1:00 PM ET)
In today’s landscape, achieving diverse participant populations is critical to ensuring that our research in clinical trials is robust. In this session, SCRS will provide an in-depth overview of the SCRS Diversity Site Assessment Tool (DSAT), a self-assessment of site capacity for recruiting and meeting the needs of diverse patient populations in clinical trials. Learn how the ‘industry gold standard’ of assessment tools will help you meet and exceed your diversity and inclusion goals.
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July 19, 2022 (12:00 PM-1:00 PM ET)
In this webinar, hear perspectives from Sponsors, CROs, sites, and patients discussing their experiences as well as challenges and opportunities regarding inclusivity in clinical research. Hear stories that have spawned into industry-wide initiatives and are currently changing the way clinical research stakeholders work together to create a more inclusive environment.
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