SITES
Navigating Participant Payment Challenges: A New Approach For Sponsors And Sites
As trials grow more sophisticated and operate on a larger, global scale, understanding the nuances of participant payment management has become essential for sponsors and sites alike.
Reduce Patient And Site Burden Through Excellence In Trial Logistics
Watch for an insightful webinar where you’ll explore the latest strategies and innovations for managing clinical trial operations with a focus on device provisioning and data workflows.
Why Relationship-Building Is The Hardest Part Of Site Success
Site owner Devora Henderson of Elevate Clinical Research reflected on her experience launching two site networks.
A Turnkey Solution For Clinical Trials In Australia
This presentation is centered on Australia's unique value proposition in the global research landscape, emphasizing its ability to deliver high-quality trials with speed and efficiency.
Korio RTSM Platform: Site User Experience
With minimal navigation, users of this platform can view a participant list, demographics, and status indicators — taking key actions like screening or randomizing without leaving the main grid.
The Advantages Of Conducting Early Phase Trials In North America
In this webinar, Altasciences discuss the similarities and differences of conducting early phase research in North America versus other geographic regions.
Automating Research Site Payments eClinicalGPS
Learn how automating payments to research sites improves research site performance, supports site sustainability and delivers a more collaborative, trusting relationship between research stakeholders.
Stay Audit-Ready: Practical Compliance Insights For Research Sites
Gain an auditors insight into common compliance gaps and learn practical ways to strengthen audit readiness in sIRB studies.
Multi-Site Capabilities For Your Phase I-II Trials
Master the complexities of renal and hepatic trials by leveraging site expertise and PK modeling to navigate recruitment challenges and ensure precise dosing for impaired patient populations.
Trends In Sponsor-Of-Choice Initiatives: Consolidating Site Payments
Listen in as leaders from Bristol Myers Squibb, CenExel Centers of Excellence, and IQVIA Technologies discuss the importance of providing a consistent clinical trial payment experience to sites.
Elevating The Site-Sponsor Experience: SaaS-Based Feasibility And Site Selection For Clinical Trials
In this webinar, learn about the transformation clinical trial feasibility and site selection across the industry.
Global Site Advocacy Group Meeting
Gain an understanding around site payment burdens and how our solutions can empower sites around the world.
Adaptive Clinical Trials
An adaptive study design can be especially useful if there are uncertainties specific to your drug. Adjusting your study as data accumulates means getting answers sooner.
The ROI Of IQVIA Site Payments
This short video explains how and why business process outsourcing (BPO) using IQVIA Technologies for site payments offers excellent ROI for sponsors and peace of mind for sites and investigators.
Sky-High Inflation And The Great Resignation: The Impact On Clinical Site Budgeting
When it comes to negotiating budgets for a clinical trial, sponsors, CROs and sites all have the same goal: to run the study. Yet just like most business relationships, the conflict comes in what defines a fair price for services rendered. Now, with inflation at its highe...
Navigating Complexities In Global Payment Operations: Best Practices For Sponsors
Deploying a successful global program for paying clinical research sites is an achievable and worthwhile goal but requires an understanding of the differences in frameworks and motivations. Learn what is needed to pays site globally in a reliable, timely, and equitable ma...
How State-Of-The-Art Clinical Trial Mobile Vision Clinics Work
Are you seeking a non-traditional option to complete the eye exams necessary for your ocular clinical trials? A mobile clinic may be the solution you're looking for.
Should Sponsors Provide Source Document Templates?
Here, we debate sponsor-provided source document templates, weighing regulatory guidance, compliance risks, and operational impacts for smarter clinical trial documentation decisions.
How Sites Are Often Evaluated By Sponsors
Adam Kinsey described how sponsor-site partnerships at Merck typically start small. Sites are evaluated not only on enrollment but on predictability and communication throughout a study.
The IQVIA Investigator Site Portal
Understand why companies are standardizing operations on a purpose-built, proven platform that empowers sites to succeed and provides sponsors with helpful insights.
Strengthening Clinical Site Partnerships For Trial Success
With the rise of site networks, the power dynamic in clinical research has shifted, making strong site-sponsor relationships more critical than ever for trial success.
Meeting Eye Exam Needs At The Point Of Need
Learn more about how mobile vision clinics supported the staff at trial sites as well as the patients through the COVID-19 pandemic and beyond.
What Boosts Efficiency At Smaller Clinical Sites?
Devora Henderson, CEO of Elevate Clinical Research, highlighted the need for clear points of contact at smaller sites.
How Merck Enhances Site Collaboration
Learn about Merck’s approach to fostering strong site relationships through specialty roles like institutional lead CRAs and site relationship managers.
Effective Study Design And Execution Of Renal And Hepatic Impairment Trials
Master the complexities of renal and hepatic trials by leveraging site expertise and PK modeling to navigate recruitment challenges and ensure precise dosing for impaired populations.
What Does Site Engagement Actually Do?
Site Engagement stays close to research sites, providing guidance, reducing administrative strain, and addressing issues early. Their support keeps studies moving by preventing small operational challenges from becoming delays.
An Overview Of Health Canada's CTA Process
Experience expedited timelines by conducting trials in Canada. Our expertise in navigating Health Canada's CTA process ensures smooth and efficient approvals.
Inside Look At Ophthalmic Early Clinical Research
Benefit from our integrated approach that combines clinical and scientific expertise specific to ophthalmology with our co-located Ophthalmic clinic.
How To Drive Stronger Sponsor-Site Partnerships
Karri Venn of SCRS discussed the value of deep partnerships, referencing a Sanofi initiative (SMILE) that trusted sites with protocol input and offered maximum budgets without negotiation.
Benefit From Enhanced Power And Intelligence
Find a supply automation value engine with intelligent automation and algorithms to analyze drug supply data and automatically adjust delivery quantities to each site based on data available in IRT.