August 4, 2020 (12:00 PM-1:00 PM)
Join this webinar to learn about generational differences in the workforce, how to maximize the millennial generations' strengths to your site's advantage, and to receive recommendations on keeping your millennial employees at your site engaged & retained.
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August 11, 2020 (12:00 PM-1:00 PM)
This session will provide key insights sponsors and sites discovered as they solved for clinical trial patient visit logistics during the COVID-19 lockdown. These considerations may provide insights for designing your disaster recovery plans.
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September 1, 2020 (12:00 PM-1:00 PM)
Building and scaling a site business during COVID-19 is challenging even now, while studies are beginning to soar again. However, even with the unpredictability posed by COVID’s ubiquitousness for the foreseeable future, Christian Burns, President of ClinEdge, will review seven tips for sites to get back on track and thrive, rather than merely survive, during this trying time.
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September 2, 2020 (12:00 PM-12:45 PM)
Join SCRS and attorney Andrew D. Goldman as he explains the updates to the Paycheck Protection Program (PPP), a loan designed to provide a direct incentive for small businesses to keep their workers on the payroll during the Coronavirus (COVID-19) crisis. If you have already received PPP, the presentation will explain what to do and the likely forgiveness application process, as the guidance is not final.
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September 9, 2020 (12:00 PM-1:00 PM)
Clinical technology is a multi-billion-dollar industry, but you’d never know it if you talked to an investigator or site coordinator running trials during the COVID-19 crisis. As sites are enrolling patients for Operation Warp Speed and other studies, many are ironically stuck in the slow lane, suffering from a lack of digital tools that could make their work more manageable in a remote model. The result: slow and labor-intensive processes that are adding costs exponentially without compensation from sponsors.
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September 15, 2020 (12:00 PM-1:00 PM)
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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September 16, 2020 (12:00 PM-1:00 PM)
This webinar will present a comprehensive overview of the origins of Sanofi's Parkinson’s Disease Functional Impacts Digital Instrument (PD-FIDI), its ongoing multi-stage R&D life cycle, and key lessons learned.
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September 17, 2020 (2:00 PM-3:00 PM)
This presentation will highlight the Seven Steps which have been designed to source, identify and select top-performing employees in a manner that increases defensibility against discriminatory claims and negligent hiring lawsuits. This presentation is a follow-on to Performisys’ May 19 SCRS webinar “Creating a High Caliber Work Culture in Clinical Site Networks™.
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September 24, 2020 (12:00 PM-1:00 PM Eastern)
The U.S. Food and Drug Administration’s Office of Women’s Health and Office of Minority Health and Health Equity will provide an overview of their efforts to advance diverse participation in clinical trials.
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September 29, 2020 (12:00 PM-1:00PM)
Do you work at a site and have concerns about competing for DCT protocols? Join the live training and gain a competitive edge by becoming Virtual Trial Capable Certified and learn the skills to adequately manage Virtual Visits with “Web-side manner” etiquette."
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November 5, 2020 (12:00 PM-1:00 PM)
Diverse patients are currently underrepresented in clinical trials and the FDA is encouraging sponsors to prioritize meeting patient diversity targets in clinical trials.
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November 10, 2020 (12:00 PM-1:00PM)
Conducting clinical research and delivering education to our youth are not often viewed as similar. However, the pandemic thrust these two typically unrelated industries into a drastic set of changes seemingly overnight. For students and teachers, it was a transition to 100% online learning with little more than a week's notice. For research sites and patients lacking tools or instructions, many opted to suspend.
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November 18, 2020 (12:00 PM-1:00 PM)
COVID-19 pandemic has created new problems and compounded existing ones faced by the global clinical research community. Without physical access to patients, the impact on data collection and patient monitoring has been significant and has forced an industry-wide initiative to re-evaluate how to manage clinical trials in this new paradigm.
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December 1, 2020 (12:00 PM-1:00 PM)
During the pandemic, RBM including remote monitoring, has been the main strategy to keep an oversight of clinical data ensuring patient safety.
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December 3, 2020 (12:00 PM-1:00 PM)
Learn from an experienced industry expert as we explore effective techniques and important understandings when it comes to negotiating a budget for an oncology study.
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December 8, 2020 (12:00 PM-1:00 PM)
Increasing the inclusion of diverse populations in clinical trials is an issue of continuing concern. How we unlock increased diversity within our trials is something that nearly every site, sponsor, CRO, and professional service provider continues to be focused on. Our presenters come to us from the sponsor and CRO perspectives to offer an insight into a successful case study where they were able to increase diversity within their clinical trials and how sites helped them to do that.
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January 12, 2021 (12:00 PM-12:45 PM)
This webinar will chart the unified mission to more patient-centric clinical trials by virtualizing, patient-centric tools currently used at sites along with the patient perspective on them.
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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.
Learn more about this event.
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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