OCTOBER'S TOP INSIGHTS! View last month's most read articles: https://lnkd.in/eAmbWcrJ Dan Schell | Jessica Cordes, Clinical Excellence GmbH | Davelyn Eaves Hood, MD, MBA, BCMAS, Rezolute, Inc., Ana Paula Tediosi, WEP Clinical | Matthew Jones, GSK, Julia Scanlon, IQVIA Technologies | Avance Clinical | Cerba Research | IQVIA Safety & Regulatory Compliance | Veristat | OpenClinica
Clinical Leader
Pharmaceutical Manufacturing
Erie, Pennsylvania 15,636 followers
A resource and forum to investigate and resolve the common struggles related to running effective clinical trials.
About us
The landscape of the life sciences industry is as vast and varied as the professionals who work in it. Some online resources aim to serve the entire space. We wish them luck. Instead, our goal is to be the most valuable resource for a specific segment of the industry – clinical research & trials – and the professionals who make their living there. The Clinical Leader community is not made up of generalists. They’re specialists, like us. We deliver in-depth content from authoritative authors and sources because that’s what our community demands. Our editors connect with and interview top clinical executives from pharmaceutical and biotech companies who share best practices, challenges faced and overcome, clinical trends, partnering strategies, and experiences implementing new technologies. Additionally, our Clinical Leader Live series of live events provides an interactive forum where sponsor companies talk about some of today's biggest challenges when managing clinical trials. Even better, the audience gets to ask questions during the presentation.
- Website
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https://www.clinicalleader.com/
External link for Clinical Leader
- Industry
- Pharmaceutical Manufacturing
- Company size
- 51-200 employees
- Headquarters
- Erie, Pennsylvania
- Founded
- 1995
- Specialties
- Clinical Trials and CRO
Updates
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Clinical trials often face unforeseen challenges that can derail progress and necessitate costly corrective efforts. However, many of these challenges can be avoided with proactive planning and early intervention. Explore the most critical steps companies can take to prevent trials from reaching a point of crisis and the importance of addressing systemic issues before they escalate. #InSeptiongroup #clinicaltrials #clinical
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Tomorrow! 🔓 Unlock new perspectives on how AI and ML can elevate clinical development efforts! Join us on November 14th at 11:00 am for a compelling discussion: "Digging Through the Hype: Can AI/ML Assist Clinical Development?" Our speakers, Brent Meyers, MBA, and Philip Ross, PhD, and Gerard Conway will share firsthand insights and demos showing how AI and ML advancements are transforming clinical trial data review and execution. Save your spot today—this is one you won’t want to miss. https://lnkd.in/e8T7Hmne If you can't make it - no worries - by registering you will receive a link to the recording so you can watch it on-demand! 💻 #clinicaldata #clinicaldevelopment #clinicaldatamangement
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Laura Hilty, a principal at HealthX Ventures, talks to Chief Editor Dan Schell about the need to better integrate data platforms and improve/enable single sign-on (SSO) solutions so sites can lessen their administrative burden. https://lnkd.in/e9mQtu5i ?utm_source=linkedin&utm_medium=social&utm_campaign=li-show-clncl-111224
Plodding Toward Better Data Integration & SSO
clinicalleader.com
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Advanced IRT/RTSM can support precision medicine’s unique challenges, allowing you to meet its goal of matching the right treatments at the right dosages for each individual patient at the right time. Discover how it’s possible to tailor RTSM to meet specific precision medicine challenges of expiry, visit & personalized shipment management. #Perceptive #RTSM #IRT
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WEBINAR TOMORROW! On November 12th, join Vinita Navadgi and Amy Koller, MBA for a deep dive into the current eConsent landscape. Discover the market's trajectory, explore IQVIA Complete Consent's cost-effective tailored solutions for all sponsors and study types, and get an exclusive look at the Interactive and Simple PDF modules highlighting new features, capabilities, and much more! 📌 Reserve your spot here: https://lnkd.in/enDqsp54
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In this week's issue, we'll explore why CROs are having to redefine their role in the outsourcing relationship, the importance of responsibly using AI in healthcare, BeiGene's unique R&D approach to get medicine to more patients, how to navigate evolving compensation models in clinical research, and other popular insights! C. Jeremy Weitz, Biogen | Stephanie Rosner, MA, PMP, DIA , Martin Hodosi, Rosanna Lim, Kearney | Mark Lanasa, BeiGene | Scout | Kym Denny Eves, Liam Eves, ReNable Research Ltd. | Citeline | Dan Schell | Worldwide Clinical Trials | ActiGraph
Why The Role Of CRO Is Changing, How BeiGene Moves Fast, Stays In-House To Conduct Its Cancer Clinical Trials, and More
Clinical Leader on LinkedIn
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The regulatory affairs function is no longer a "one size fits all" function; the decision to outsource or insource the function is growing more complex, and specific AI tools can help regulatory processes. Explore insights on what the future of regulatory affairs may entail and how to succeed in that role: https://lnkd.in/eeHxvTBX By Maggie Chan, Nora Hernández García, and Hilde Viroux, PA Consulting
The Regulatory Affairs Function Is Evolving. Are You Evolving With It?
clinicalleader.com
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🔍Curious about the potential of AI and ML 🤖 in clinical trials? Join us on November 14, 2024, at 11:00 AM to explore real-world approaches for leveraging AI to streamline clinical data management and drive smarter, faster decision-making. In this session, our experts will walk you through: ✔ Innovative data automapping using ML to flag non-mappable data, allowing teams to focus on critical resolution efforts. ✔ Practical insights into using Generative AI for identifying patterns and hypotheses—while balancing the regulatory caution required. ✔ Human-in-the-loop strategies that maximize data quality, enabling a shift from routine tasks to high-impact analysis. Speakers: 👤Brent Meyers, MBA, Exec. Director, Clinical Analytics, Revvity Signals 👤Philip Ross, PhD, Strategic Clinical Analytics, Revvity Signals 👤Gerard Conway, Data Analytics and Spotfire Expert, Revvity Signals Reserve your spot and learn more here: https://lnkd.in/eps2MZb8 #clinicaldata #clinicaldatamangement #clinicaldevelopment
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The messaging about your clinical trial starts before the trial, but Denise N. Bronner, Ph.D. says the kind of information you need to be conveying may not be what you would expect... Watch the discussion: https://lnkd.in/eHyXEbzQ
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