Archive available until Dec 21, 2019
With the number and complexity of clinical trials increasing significantly, the percent of the clinical research workforce that is disengaged is significant. Coordinators are overburdened and sites cannot afford high turnover. There is a massive talent shortage within the clinical research field and sites are struggling to hire smart and improve performance. Sites can identify the right talent and keep them through better hiring skills and a strong supportive culture. The outcome of a good hire and site culture is higher profitability and productivity, which every site can use in this challenging research market.
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Archive Available until March 6, 2020
The clinical research industry is changing at a truly remarkable pace. With the incorporation of new technology, increased trial complexity and tightening profit margins, the relationship between the site and their industry partners has never been more important. With more than 200,000 clinical trials currently underway and the number of sites decreasing globally for a variety of reasons, the industry continues to miss timelines even when first-to-market compounds are critical in order to remain competitive. As this changing landscape allows for sites to become more selective of who they choose to work with, now is the time to come together and dig into the specifics that are of critical importance as sites select the industry partners they choose to work with.
In response, SCRS has developed a 5-part webinar series that outlines how sponsors and CROs can best address these issues and become a sponsor or CRO of choice. This series will provide SCRS partners with an opportunity to hear directly from the sites what drives them toward partnerships and learn how to position your company as a sponsor or CRO of choice.
We invite you to join SCRS and our top member sites for a constructive discussion that will outline how the industry can support continued site growth and how to be identified as a sponsor or CRO of choice.
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Archive Available until March 6, 2020
The clinical research industry is changing at a truly remarkable pace. With the incorporation of new technology, increased trial complexity and tightening profit margins, the relationship between the site and their industry partners has never been more important. With more than 200,000 clinical trials currently underway and the number of sites decreasing globally for a variety of reasons, the industry continues to miss timelines even when first-to-market compounds are critical in order to remain competitive. As this changing landscape allows for sites to become more selective of who they choose to work with, now is the time to come together and dig into the specifics that are of critical importance as sites select the industry partners they choose to work with.
In response, SCRS has developed a 5-part webinar series that outlines how sponsors and CROs can best address these issues and become a sponsor or CRO of choice. This series will provide SCRS partners with an opportunity to hear directly from the sites what drives them toward partnerships and learn how to position your company as a sponsor or CRO of choice.
We invite you to join SCRS and our top member sites for a constructive discussion that will outline how the industry can support continued site growth and how to be identified as a sponsor or CRO of choice.
learn more...
Archive Available until March 6, 2020
The clinical research industry is changing at a truly remarkable pace. With the incorporation of new technology, increased trial complexity and tightening profit margins, the relationship between the site and their industry partners has never been more important. With more than 200,000 clinical trials currently underway and the number of sites decreasing globally for a variety of reasons, the industry continues to miss timelines even when first-to-market compounds are critical in order to remain competitive. As this changing landscape allows for sites to become more selective of who they choose to work with, now is the time to come together and dig into the specifics that are of critical importance as sites select the industry partners they choose to work with.
In response, SCRS has developed a 5-part webinar series that outlines how sponsors and CROs can best address these issues and become a sponsor or CRO of choice. This series will provide SCRS partners with an opportunity to hear directly from the sites what drives them toward partnerships and learn how to position your company as a sponsor or CRO of choice.
We invite you to join SCRS and our top member sites for a constructive discussion that will outline how the industry can support continued site growth and how to be identified as a sponsor or CRO of choice.
learn more...
Archive Available until March 6, 2020
The clinical research industry is changing at a truly remarkable pace. With the incorporation of new technology, increased trial complexity and tightening profit margins, the relationship between the site and their industry partners has never been more important. With more than 200,000 clinical trials currently underway and the number of sites decreasing globally for a variety of reasons, the industry continues to miss timelines even when first-to-market compounds are critical in order to remain competitive. As this changing landscape allows for sites to become more selective of who they choose to work with, now is the time to come together and dig into the specifics that are of critical importance as sites select the industry partners they choose to work with.
In response, SCRS has developed a 5-part webinar series that outlines how sponsors and CROs can best address these issues and become a sponsor or CRO of choice. This series will provide SCRS partners with an opportunity to hear directly from the sites what drives them toward partnerships and learn how to position your company as a sponsor or CRO of choice.
We invite you to join SCRS and our top member sites for a constructive discussion that will outline how the industry can support continued site growth and how to be identified as a sponsor or CRO of choice.
learn more...
Archive Available until March 6, 2020
The clinical research industry is changing at a truly remarkable pace. With the incorporation of new technology, increased trial complexity and tightening profit margins, the relationship between the site and their industry partners has never been more important. With more than 200,000 clinical trials currently underway and the number of sites decreasing globally for a variety of reasons, the industry continues to miss timelines even when first-to-market compounds are critical in order to remain competitive. As this changing landscape allows for sites to become more selective of who they choose to work with, now is the time to come together and dig into the specifics that are of critical importance as sites select the industry partners they choose to work with.
In response, SCRS has developed a 5-part webinar series that outlines how sponsors and CROs can best address these issues and become a sponsor or CRO of choice. This series will provide SCRS partners with an opportunity to hear directly from the sites what drives them toward partnerships and learn how to position your company as a sponsor or CRO of choice.
We invite you to join SCRS and our top member sites for a constructive discussion that will outline how the industry can support continued site growth and how to be identified as a sponsor or CRO of choice.
learn more...
Archive Available until March 5, 2020
Understanding the ins and outs of research billing compliance and research billing regulations can be a difficult task, but with the proper knowledge of these subjects, researchers can successfully apply appropriate billing practices.
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Archive Available until March 26, 2020
Join this webinar to learn the primary tools and best practices utilized by hospital-based research sites that will empower your team members to utilize consistent, clear and effective communication strategies.
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Archive Available until March 28, 2020
Join PAREXEL for a discussion on contracting and budgeting in Poland.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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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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.
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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.
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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.
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