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.
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July 9, 2019 (12:00 PM-1:00 PM)
Thursday, July 11, 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.
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Tuesday, July 16, 2019 (12:00 PM-1:00 PM)
Tuesday, July 23, 2019 - Thursday, July 23, 2020
July 30, 2019 (12:00 PM-1:00 PM)
The webinar will be focused on how sites can use the newest social media patient engagement tactics to boost patient recruitment. We will take a deep dive into what many successful research sites are doing to be top enrollers and build strong patient community connections.
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Tuesday, August 6, 2019 (12:00 PM-1:00 PM)
August 20, 2019 (12:00 PM-1:00 PM)
Sponsors, CROs and investigative sites all have an equally important role in ensuring the success of clinical trials. Just as crucial to clinical trial success is the role of technology; however, much remains to be learned in order to utilize it appropriately to increase performance, collaboration and satisfaction for all parties involved. Are sponsors and CROs ensuring that their protocols are site-centric? Can sites better leverage technologies they already use to take on a more proactive role in clinical research? In this webinar, we will showcase technology-created opportunities, from protocol development to study closeout, that help create stronger relationships.
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Tuesday, August 27, 2019 (12:00 PM-1:00 PM)
Instances of cybercrime are on the rise. Is your site prepared to navigate it, or are you a potential victim? Brought to you by Hylant - FBI, supervisory special agent (retired) Scott E. Augenbaum will walk through case studies surrounding cybercrime issues and threats that clinical research sites and life sciences organizations face every day. Augenbaum has responded to 1000s of cybercrime incidents during his three decades with the FBI, including numerous victims from healthcare, bio-technology and life sciences organizations. This webinar will present case studies and utilize non-technical language to reinforce the importance of knowing how to identify cybercrime and protect your organization.
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Wednesday, September 4, 2019 (12:00 PM-1:00 PM)
Tuesday, September 17, 2019 (12:00 PM-1:00 PM)
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.
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Wednesday, December 4, 2019 (12:00 PM-1:00 PM)