Partnering Webinars
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What Boosts Efficiency At Smaller Clinical Sites?
4/25/2025
Devora Henderson, CEO of Elevate Clinical Research, highlighted the need for clear points of contact at smaller sites.
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Tailored Sponsor Engagement Key To Unlocking Site Network Efficiency
4/25/2025
Karri Venn, VP site advocacy and mentorship at SCRS, emphasized the importance of sponsors recognizing the structure and capabilities of larger site networks.
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Unlocking Continued Revenue And Growth From Established Products
4/14/2025
Gain insights into how pharmaceutical companies successfully handle post-approval regulatory upkeep for established products, focusing on reducing operational costs and expanding global market access.
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Critical Imaging Risks In GLP-1 And Neurology Studies
4/3/2025
In the evolving landscape of GLP-1 and neurology clinical trials, imaging has become a pivotal tool for evaluating both efficacy and safety. Delve into the early indicators of imaging-related challenges and insights into preclinical strategies for effective risk mitigation.
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Elevating The Site Voice
3/27/2025
A decentralized trial can be daunting for sites, but Medidata offers solutions to help site staff, sponsors, and patients move smoothly through the clinical trial process.
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Who's In Charge? How To Ensure Effective Trial Oversight, Leadership
3/19/2025
Gain valuable insights into the role of sponsor-side Clinical Operations leadership, the risks of over-relying on CROs, and key strategies for fostering collaboration between sponsors and partners.
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Clinical Research Workforce Faces Growing Shortages
3/14/2025
In this clip, Elisa Cascade of Advarra discusses a survey on the clinical research workforce found a 41% shortage of PIs across sites, with even greater shortages among CRCs. Nearly two-thirds reported staffing issues, threatening research sustainability. Most respondents believed the situation would worsen rather than improve, raising concerns about future workforce stability.
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Financials Of Clinical Research Still A Deterrent To PIs
3/14/2025
According to Jimmy Bechtel of SCRS, part of the one-and-done PI problem is the financials associated with clinical research.
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Is The BMIS Dataset Flawed For This Use?
3/14/2025
The BMIS dataset, which tracks FDA Form 1572 submissions, is incomplete and voluntary, making it difficult to assess the true number of "one and done" PIs. Explore how past surveys have raised doubts about using the Form 1572 metric to measure retention of PIs.
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CTTI Survey Identifies Why Many PIs Drop Out After One Trial
3/14/2025
Morgan Hanger of CTTI discusses their survey of 201 PIs in FDA-regulated drug trials that indicated over half (108) participated only once in a trial, citing time constraints, workload, safety reporting, and financial burdens were why they did not continue. Despite these challenges, 44% wanted to continue but lacked opportunities, suggesting a disconnect in trial recruitment.