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 12, 2022 (12:00 PM-1:00 PM ET)
The importance of investigator sites in patient diversity and inclusion efforts can’t be overstated. In this session, hear how to support and grow your site’s team to influence the success of your diverse recruitment practices as well as strategies underway at Pfizer to advance diversity within clinical trials.
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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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August 2, 2022 (12:00 PM-1:00 PM ET)
In this informative discussion, we’ll look at the narrative and pivot of clinical trials and a much needed industry focus on diversity and equity since COVID-19. We’ll share real-world examples of how one top pharmaceutical company sought opportunities to work with diverse patient populations using clinical intelligence covering HCPs and investigators, institutions and sites, therapeutic areas, patient populations, and sponsors.
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August 16, 2022 (12:00 PM-1:30 PM ET)
As various medical devices, drugs, and other lifesaving technology come to market, the clinical research industry has to focus on ensuring our work is inclusive of all so our products can bring optimal health to all. This webinar seeks to discuss racial diversity in clinical trials and how industry stakeholders can work together to increase awareness, participation, and advance health equity.
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August 23, 2022 (12:00 PM-1:00 PM ET)
This webinar will discuss how budgeting and financial terms often takes a tremendous amount of time – sometimes, even becoming the most time-consuming activities pre-study. As the clinical research industry continues to change, sites need to continuously adapt their costs to align with client demands including remote monitoring, remote patient visits, and increasing labor costs. During this session, site budget experts will share their budget checklist and strategies to ensure you never miss another line item in your study budget. Hear from sites that manage this well and learn ways to speed up your budget execution.
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September 20, 2022 (12:00 PM-1:00 PM ET)
A site’s role in a DCT is crucial - they are the frontline for patients and play many roles: trainer, helpdesk, protocol consultant, etc. Have you wondered what has changed for sites conducting DCTs since 2020? Medidata has the details on the ways technology usage has increased in the last two years and the changes sites still want to see to streamline decentralization. This webinar provides a summary of data on DCTs collected from sites within the SCRS community in 2020 and 2022.
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September 27, 2022 (12:00 PM-1:00 PM ET)
Behavioral science aims to understand, explain, and predict human behavior and decision-making. It helps us understand that patients are heterogeneous in terms of underlying preferences, attitudes, history, and values, which can impact their engagement in clinical trials. This webinar will highlight how behavioral science can impact patient engagement from recruitment to retention.
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October 18, 2022 (12:00 PM-1:00 PM ET)
In this session, learn what it means to utilize technology in clinical trial contracting. Innovative technologies can help your site understand and apply historical data and trends to make the contracting process less tedious and time consuming for all stakeholders. Join us to learn how to extend your knowledge in budgeting and contracting at your site.
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October 25, 2022 (12:00 PM-1:00 PM ET)
The reality of a clinical trial is what happens at the site. This makes the site’s feedback extremely valuable and very necessary. Raising the site's voice in the industry is a huge priority for Medidata and we are here to report back trends and solutions based on data and feedback received during our engagement with sites over the last year.
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November 8, 2022 (12:00 PM-1:00 PM ET)
Clinical trial sites and patient advocates must align on the value of research to achieve diversity, equity and inclusion. This session will be a practical discussion about what diversity, equity and inclusion really mean both to research sites and patient advocates. We will highlight new research sponsored by Teckro and conducted by the Center for Information and Study on Clinical Research Participation (CISCRP) to look at the nuanced complexities that can prevent LGBTQ+ community participation. The report will be shared with webinar attendees.
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November 15, 2022 (12:00 PM-1:30 PM ET)
The current landscape is driving many sponsors to redefine their site and recruitment strategy to address the lack of diverse representation in clinical trials. This has left many sites wondering if they have the right attributes to be considered for inclusion on upcoming trials and if sponsors are willing to provide resources to help them fill in DEI gaps. During this webinar, Janssen will discuss what they are looking for in sites and how they are empowering sites to achieve DEI goals in the current and upcoming trial pipeline.
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