January 19, 2021 (12:00 PM-12:45 PM)
More and more healthcare institutions globally are trying to increase their research portfolio, but engagement of busy physicians is always a challenge. In this webinar, we will discuss strategies to engage physicians to conduct research, ways to increase visibility of research institution-wide, and the support that physicians need in order to feel comfortable committing to research.
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February 9, 2021 (12:00 PM-1:00 PM)
More and more healthcare institutions globally are trying to increase their research portfolio, but engagement of busy physicians is always a challenge. In this webinar, we will discuss strategies to engage physicians to conduct research, ways to increase visibility of research institution-wide, and the support that physicians need in order to feel comfortable committing to research.
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March 7, 2021 (8:00 PM-9:00 PM ET)
What can we learn from past epidemics to help manage the COVID-19 pandemic more efficiently and effectively? Explore how Taiwan is being recognized for its work to combat the COVID-19 pandemic.
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April 6, 2021 (12:00 PM-1:00 PM ET)
Oncology is a fast-growing therapeutic area with increasing complexities in clinical trial design. This leads to a complex regulatory process, low patient enrollment and increased cost. In order to better understand these complexities and build efficiencies, a multifaceted approach toward solutions is necessary. In this panel discussion, we will take into account the patient’s voice and the physician’s standpoint, and discuss study operations from site and sponsor perspectives. Partnering with each stakeholder and having a collaborative approach is the only way to find solutions. Let’s start here.
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April 13, 2021 (12:00 PM-1:00 PM ET)
Virtual training and site engagement tools are evolving to provide increasingly meaningful support for clinical research Investigators and study Sponsors. Join us for a discussion of how these platforms and the programs they deliver can facilitate trial conduct, enhance Site performance, and yield improved outcomes from the Sponsor and Site perspective.
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April 15, 2021 (12:00 PM-1:00 PM ET)
The participation of minority study candidates in clinical trials remains low. Many incentive programs have been put in place across clinical trial sites to improve enrollment and participation Learn from both sites and patient directly on what is working and how to overcome barriers that lessen inclusion into trials.
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April 27, 2021 (12:00 PM-1:00 PM ET)
Conducting clinical trial feasibility is one of the first steps in study start up. This process includes the critical components of aligning on the study design and assessing potential study sites’ qualifications and capabilities
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May 4, 2021 (10:00 AM-11:00 AM ET)
Greenphire, a leader in clinical trial financial automation, will host this interactive panel to take a deeper dive into trends today, and how technology together with training is driving towards the future of clinical trials, now.
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May 11, 2021 (12:00 PM-1:00 PM ET)
In this webinar, presenters will describe innovative methods applied within clinical development to Advance Patient engagement in R&D through 4 perspectives: Direct patient engagement, patient informed development, digital patient engagement, and behavioral science. These four perspectives will address the gaps and needs in patient empowerment, evolution to decrease site burden, and increase access to clinical trials.
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May 18, 2021 (12:00 PM-1:00 PM ET)
Key performance indicators (KPI) provide sites evidence-based metrics to promote the health of their research sites. Monitoring KPI's offers an in-depth risk-based assessment to analyze and identify areas of practice to strengthen clinical research trial operations. As time is of the essence when deploying clinical trials, a site's ability to be agile with data metrics offers sponsors and CRO quick implementation timelines based on a site's past performances validated by KPIs. We will discuss how to categorize, track, measure, and implement quality indicators within your business and clinical operation to monitor and track your KPIs during this session.
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May 27, 2021 (12:00 PM-1:00 PM ET)
In this webinar, we are going to discuss how and why we need to go beyond the need for more Diversity in Clinical Trials. We will discuss how the Industry is collaborating on this important topic with real examples from Dr. Popa McKiver from BMS who will discuss the joint work, and recommendations, done by FDA, AACR and working groups to address patient diversity in multiple myeloma. During this discussion, we will also discuss the physician perspective from past to present and sponsor driven programs to make these efforts sustainable.
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June 29, 2021 (12:00 PM-1:00 PM ET)
Validation of your eClinical systems may not be something all are familiar with, though it is a very useful step to ensure a quality solution. What tools are available? Do I need a tech degree to run it? It is especially important to understand the overall quality of the system you use to store and manage your regulatory data. In this session we will discuss the best practices for electronic implementation, maintaining audit readiness, and FDA expectations for electronic systems, including how the right tools can strengthen your overall compliance processes.
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July 13, 2021 (12:00 PM-1:00 PM ET)
Does the General Data Protection Regulation (GDPR) and other modern data protection regulations affect you and your investigator site? Attend this webinar to learn how GDPR and state-by-state data protection regulations like the California Consumer Privacy Act (CCPA) affect healthcare and clinical research business including sites, sponsors, CROs, universities and other industry stakeholders and what you can do to be in compliance today.
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July 20, 2021 (12:00 PM-12:45 PM)
The U.S. Food and Drug Administration’s Office of Women’s Health and Office of Minority Health and Health Equity aims to advance the inclusion of women and minority populations in clinical trials. This webinar will provide an overview of their efforts to advance diverse patient participation, address related policy strategies and describe the communication and outreach efforts that the FDA is using to ensure minority populations and women are adequately represented.
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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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