Tuesday, July 16, 2019 (12:00 PM-1:00 PM)
How to better engage with patients in a continual manner to stimulate education and engagement with clinical research before, during, and beyond clinical trials.
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July 23, 2019 (12:00 PM-1:00 PM)
Currently, limited best practices exist for sites to prepare for mobile clinical trials and engage patients throughout the process. CTTI’s Mobile Clinical Trial (MCT) Engaging Patients and Sites (EPS) recommendations provide a needed roadmap for how to engage patients and sites in mobile trials. The speakers will discuss best practices sites can utilize to prepare for the implementation of mobile clinical trials and set themselves and patients up for a positive experience.
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Tuesday, August 6, 2019 (12:00 PM-1:00 PM)
Although oncology protocols are complex, principal investigators play a pivotal role since they are responsible for the entirety of each research study. Within this webinar, you will learn about varying techniques that will enable PIs for success. With constant decision making that affects a trial, whether it is direct or through delegation, there is a need to focus efforts on an organization’s greatest potential. By understanding how to identify, qualify and retain PIs, sites and sponsors can expand their talent pool and have an increased level of engagement within clinical research.
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Tuesday, August 13, 2019 (12:00 PM-1:00 PM)
Topics addressed focus on Human Resource activities essential to operating a professional and successful research enterprise.
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August 20, 2019 (12:00 PM-1:00 PM)
Part of the ongoing Diversity Series, offered at no charge to members and non-members. Medidata will present an overview of key issues sites face today with respect to recruitment and engagement of diverse populations for clinical research. Leading patient advocates will join Medidata to provide their perspectives and insights on how sites can build stronger relationships in their communities. Medidata will also share ongoing activities the company has undertaken to encourage more diverse clinical trials.
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Wednesday, September 4, 2019 (12:00 PM-1:00 PM)
This webinar will focus on examining various aspects of Decentralized Trials, including; the FDAs position, a history of what has worked and what hasn't, and the role that sites play in successful implementation. Attendees will gain a deeper understanding of decentralized services that are currently available and being utilized, the outcomes that have been achieved, and how sites can leverage them to increase their enrollment and improve their retention of patients in clinical trials.
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September 10, 2019 (12:00 PM-1:00 PM)
Multiple surveys have found that investigators and clinical site staff underestimate and are not prepared for the effort involved in getting paid for their services in research trials. While most have the skills they need to streamline the process, they may lack the practical knowledge for establishing sound practices upfront and resolving issues that may arise later. This webinar will show investigators and site staff how they can best work with the sponsor, CRO or third-party vendors to secure favorable contract terms and streamline the payment process.
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Recording available until September 19, 2020
The number of clinical systems, including Interactive Response Technologies (IRTs), is seemingly always increasing. This introduces difficulties to sites as they try to make each system fit within their workflow. There are more passwords to keep track of, more training required and more time spent away from the patient contacting help desks.
Despite these difficulties, tremendous value can be obtained from utilizing an IRT, especially within highly complex trials such as oncology. What is needed is an IRT designed to meet the needs of the site. This webinar will discuss how sites can influence the value of their IRT, and identify ways to proactively impact its design.
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Recording available until September 26, 2020
Jason Bork from the Global Alzheimer's Platform Foundation and Rick Ward from Trifecta Clinical will lead a discussion about how the GAP Foundation is leveraging technology to dramatically reduce the need for redundant rater training/certification by centrally managing certification status and allowing all study sponsors to access this documentation in support of their respective clinical trial programs.
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Recording available until Tuesday, October 22, 2020
Attendees will learn about TransCelerate’s Common Protocol Template Initiative and how we are interacting with industry stakeholders and regulators to create and maintain a model clinical trial protocol template.
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Recording available until October 24, 2020
With rapid advances in technology and science, the importance of representative populations in clinical trials and biomedical research is paramount. This webinar will focus on strategies to address disparities in clinical research and promote the promise of personalized healthcare for all patients.
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Recording available until Thursday, October 31, 2020
Remote monitoring saves sponsors time and money, but what are the risks and rewards encountered by sites? The purpose of this webinar is to define and explain what risk-based and remote monitoring are and to share the best practices. The two speakers will cover “both banks of the river”- site point of view and experience and also CRO/Sponsor point of view and experience.
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Recording available until November 12, 2020
One of the main causes of study start-up delays- a notorious bottleneck in clinical trials- is inefficient collaboration between sponsors/CROs and sites. Transforming study start-up requires that sites and sponsors/CRO's alike adopt a paradigm shift utilizing both technology and other industry initiatives.
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Recording available until November 26, 2020
This webinar will review the new features and associated best practices that will save time and allow sites and larger organizations to prepare in advance for a significant increase in the number of studies to be run in SIP in 2020.
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Recording available until December 4, 2020
Negotiating clinical trial agreements can appear to be an intimidating undertaking, but it does not have to be. Understanding the legalese and uncovering budget pitfalls before signing on the dotted line.
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Recording available until December 17, 2020
Join us for another installment of our Diversity Series, featuring presenters from FDA. The FDA Office of Minority Health and Health Equity will provide an overview of their office and the work they are doing to advance clinical trial diversity.
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Recording available until December 19, 2020
Join this interactive discussion from industry leaders on how to overcome common technology challenges and best practices for adopting eRegulatory to increase efficiency, improve compliance, and grow study capacity.
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Recording available until January 9, 2021
With the industry trending toward the site partnership model, how can your site ensure that it is included and stands out among the rest? What are sponsors and CROs looking for when identifying a site for study partnership? This webinar will answer these questions, and help you highlight your site’s capabilities to drive new business and be awarded more studies – that you actually want!
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Available until January 14, 2021
Right now, over 2 million patient volunteers in the United States are participating in clinical trials which does not come close to the 58 million patient volunteers needed. Javara’s Integrated Research Organization (IRO) model transforms the clinical research ecosystem.
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Archive available until January 23, 2021
While addressing findings in monitoring reports is an important step in the audit preparation process, a thorough quality improvement programs is required to address deficiencies across the organization. The peer-to-peer chart review process is one tool which can be implemented to improve study integrity and data accuracy at your organization.
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Archive Available until February 25, 2021
CTA budget negotiations are a necessary evil, which ultimately, are just another roadblock standing in the way of patients who need care. This webinar will identify strategies to remove some of the mystery and expedite processes.
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March 17, 2020 (12:00 PM-1:00 PM)
Join this webinar to learn best practices and common mistakes to avoid when transitioning to electronic regulatory binders. You will gain insights from industry experts and learn from others that have made the transition to ensure success.
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Tuesday, April 14, 2020 - Wednesday, April 14, 2021
This webinar will explain what it means to have an online presence that precipitates patient feedback and site optimization.
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May 7, 2020 (12:00 PM-1:15 PM)
In this webinar hosted by SCRS and ACRP, two attorneys will explain some of the new and existing legislation designed to protect American workers and aid small businesses.
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May 12, 2020 (12:00 PM-1:00 PM)
Join representatives from Syneos Health and Elligo Health Research to learn about the benefits of such an approach, and the ways in which research organizations can ensure quality and promote patient access to clinical trials.
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May 14, 2020 (12:00 PM-1:00 PM)
In this webinar we’ll look at how Artificial Intelligence (AI) technology is fundamentally changing clinical trial development, feasibility, and recruitment.
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May 19, 2020 (1:00 PM-2:00 PM)
What if you never had to “manage” your people? Discover a results-driven performance approach proven to deliver immediately implementable ideas that enable you to leverage the talent of an individual, a team or an entire organization.
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Wednesday, May 20, 2020 12:00 pm Australia Eastern Standard Time (Sydney, GMT+10:00)
Hosted by the Society of Clinical Research Sites’ (SCRS) Diversity Awareness Program, this webinar will explore the current diversity barriers in clinical trials and the best practices that can be implemented to overcome these.
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May 21, 2020 (12:00 PM-1:00 PM Eastern)
As members of SCRS Diversity committee, representatives from Emerson Clinical Research and Medidata will present an overview of key issues facing sites today with respect to recruitment and engagement of diverse populations for clinical research. Patient advocates will provide their perspectives and insights on how sites can build stronger relationships in their communities.
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Wednesday, May 27, 2020 10:00 am Singapore Time (Singapore, GMT+08:00)
What can we learn from past epidemics to help manage the COVID-19 pandemic more efficiently and effectively? Explore how the difficulties and losses experienced during the SARS outbreak of 2003 shaped Taiwan to be recognized as one of the countries that other states are beginning to learn from as the world fights this COVID-19 pandemic.
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Available until June 9, 2021
Our latest talk on social media breaks down, step-by-step, the latest techniques for patient recruitment, retention and advocacy across the new and old platforms including: Snapchat, Instagram and Facebook.
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Available until June 11, 2021
The interpretation of genomic test results is challenging for those untrained in this field. This results in lack of awareness for treating oncologists, overworked genetic counselors and molecular team leads resulting in patients missing opportunities to be prescribed potentially life saving precision therapies.
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June 16, 2020 (12:00 PM-1:00 PM)
Join us as Marie E. Lamont from Intelliquet outlines key challenges with EMR Recruitment and various ways to address them.
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