Tuesday, April 16, 2019 - Thursday, April 16, 2020
PatientWise will discuss methods for sites to achieve and sustain credibility within their community, and cost-effective tactics such as community outreach and social media to increase patient referrals and meet enrollment goals.
Learn more about this event.
Thursday, April 18, 2019 - Saturday, April 18, 2020
With rapid advances in technology and science, the importance of representative populations in clinical trials and biomedical research is paramount.
Learn more about this event.
Wednesday, April 24, 2019 - Friday, April 24, 2020
This webinar will highlight common payment challenges among sites and indicate how to improve workflows for increased efficiency and optimization.
Learn more about this event.
Thursday, May 2, 2019 - Saturday, May 2, 2020
Join SCRS and Molly Downhour from Medix for a presentation on the hiring challenges faced by oncology research sites.
Learn more about this event.
Tuesday, May 7, 2019 - Thursday, May 7, 2020
Despite scientific advances, oncology clinical trials are still challenged by delayed trial timelines, slow site activation and poor patient enrollment. To overcome these barriers, we need to redefine the site activation paradigm and our ability to influence the process.
Learn more about this event.
Tuesday, May 14, 2019 - Thursday, May 14, 2020
This presentation will explore the current and future state of clinical trials, remote clinical trials and their impact on you, and how to prepare to integrate new technologies and processes into your site.
Learn more about this event.
Tuesday, May 21, 2019 - Thursday, May 21, 2020
Using a system for regulatory documents can be the start down the path to becoming paper free.
Learn more about this event.
Tuesday, May 28, 2019 - Thursday, May 28, 2020
There is much talk about siteless trials. Are sites aware? What is the solution to remain sustainable?
Learn more about this event.
Thursday, June 20, 2019 - Saturday, June 20, 2020
Diversity in clinical trials is becoming a top priority at many sponsor companies thanks to efforts by regulatory authorities, the changing landscape of drug development and advancing scientific approaches to find effective treatment options. In this webinar we will explore strategies and tactics that both sites and sponsors can use and, more importantly, how they can work together to ensure that diverse and representative samples of participants are enrolled into their clinical programs.
Learn more about this event.
Tuesday, June 25, 2019 (12:00 PM-1:00 PM)
Tuesday, July 2, 2019 (12:00 PM-1:00 PM)
Electronic source (eSource) is becoming increasingly popular with clinical research sites, but many site operators are uncertain whether to embrace it. This webinar will discuss the growing adoption of eSource and position it in context of broader industry trendlines such as site consolidation and rising venture interest in clinical research technology. The speaker will share lessons learned from the past several years and predictions on where the industry is headed. Site directors from two research institutions will provide concrete examples of their experience implementing and utilizing eSource, and the challenges they had to overcome.
Learn more about this event.
July 9, 2019 (12:00 PM-1:00 PM)
Educating your community on clinical research is essential to increasing involvement in clinical trials. The more actively your site is involved in outreach and awareness efforts, the more successful your site’s recruitment efforts will be. During this webinar, sites will gain an understanding of how to effectively impact their community by engaging in alternative outreach methods rather than the more traditionally utilized means. Strategies to ensure your community knows who you are, why you exist and why clinical trial participation is important will be explored.
Learn more about this event.
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.
Learn more about this event.
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.
Learn more about this event.
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.
Learn more about this event.
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.
Learn more about this event.
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.
Learn more about this event.
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.
Learn more about this event.
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.
Learn more about this event.
Thursday, September 19, 2019 (12:00 PM-1:00 PM)
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.
Learn more about this event.
September 24, 2019 (1:00 PM-2:00 PM)
A panel of site-centric industry organizations will present and discuss the findings from a new study aimed at addressing these questions about single sign-on, disparate systems, site networks, site selection, and the hottest topic for sites right now - decentralized trials.
Learn more about this event.
Thursday, September 26, 2019 (12:00 PM-1:00 PM Eastern Standard Time)
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.
Learn more about this event.
Tuesday, October 22, 2019 (12:00 PM-1:00 PM)
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.
Learn more about this event.
October 24, 2019 (12:00 PM-1:00 PM)
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.
Learn more about this event.
Thursday, October 31, 2019 (12:00 PM-1:00 PM)
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.
Learn more about this event.
November 12, 2019 (12:00 PM-1:00 PM)
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.
Learn more about this event.
November 26, 2019 (12:00 PM-1:00 PM)
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.
Learn more about this event.
Wednesday, December 4, 2019 (12:00 PM-1:00 PM)
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.
Learn more about this event.
December 17, 2019 (3:00 PM-4:00 PM)
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.
Learn more about this event.
December 19, 2019 (12:00 PM-1:00 PM)
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.
Learn more about this event.
Thursday, January 9, 2020 - Saturday, 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!
Learn more about this event.
Tuesday, January 14, 2020 - Thursday, 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.
Learn more about this event.
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.
Learn more about this event.
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.
Learn more about this event.
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.
Learn more about this event.