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Complexity to Catalyst: Building Site Readiness, Resilience & Innovation
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AI & Digital Health: Advancing Access & Innovation in Latin American Trials
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Health Literacy in Action: The Impact of Plain Language Communication in Clinical Research
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Advancing Access: How SaaS is Transforming Clinical Trials
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Advancing Imaging in Clinical Trials Using AI
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Future-Ready Research: Optimizing Sites for Continued Success
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Harnessing Generative AI in Clinical Research
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AI in Clinical Trials: Unlocking the Potential
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Breaking Down Site Complexities and Start-Up Barriers in Clinical Trials
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From Patient Care to Discovery: A Clinician's Journey into Research
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Inside MAGI: Innovation, Education, and Industry Trends
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Revolutionizing Clinical Research Through Collaboration and Innovation
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Have a Safe Trip: Clinical and Patient Alignment in Research with Psychedelics
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Breaking Barriers: Reasons to Expand Site Cancer Trial Portfolios
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Patient Advocacy Advancing Breakthrough Science and Community Engagement
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Guarding Research Integrity: The IRB's Essential Role
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Addressing Challenges in Site Feasibility
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Ethical Review and AI in Clinical Trials
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Addressing Measurement Challenges for PTSD Trials with Technology
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What Is E-Consent? Interview with Erin Brower
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Creating Partnerships: Aligning Vendor Support for Success in Clinical Research
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WCG's IRB Policy Change: Harmonizing Consent (Part 2)
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WCG's IRB Policy Change: Harmonizing Consent (Part 1)
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The Ethical and Safety Considerations of Accelerating Oncology Trials
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Embarking on a Research Revolution – A Conversation with Florence Healthcare
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The CRA’s Evolving Role in a Postpandemic Industry
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MAGI@home: Practical Intelligence, Real-life Examples, Actionable Information
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Diversity & Inclusion with Technology in Decentralized Trials
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Amplifying Patient Voices to Advance Clinical Research: The Importance of Patient Advocacy
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The Importance of Diversity, Equity, Inclusion, and Intersectionality in Clinical Research
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Delve into the World of Psychedelic Research and Ethical Inquiry
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A 360-degree View on Motivators and Deterrents to Clinical Trial Participation
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Breaking Down Enrollment Barriers: How DE&I, Technology, and Protocol Design Impact Enrollment Success
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Unlocking Site Potential: Reducing Site Burden and Enhancing Clinical Trial Efficiency
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Connecting Patients to Trials: Bernadette Siddiqi of The Michael J. Fox Foundation for Parkinson’s Research
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On the Future of Movement Disorder Trials: Part 4 of WCG’s Transforming CNS Trials Series
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Prostate Cancer Survivor Bryce Olson’s Message: “Sequence Me!”
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On the Future of Depression Trials: Part 3 of WCG’s Transforming CNS Trials Series
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LaTasha H. Lee, PhD, MPH: Advocating for Health Equity, Advancing Sickle Cell Disease Research
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Jeffrey Borghoff: Finding Joy and Purpose after an Early-Onset Alzheimer’s Diagnosis
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On the Future of Schizophrenia Trials: Part 2 of WCG’s Transforming CNS Trials Series
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Lisa Deck: Young Stroke Survivor Transforms Life-Altering Challenge into Purpose-Driven Advocacy for Others
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The Case for Centralized Monitoring: Optimizing Data Quality and Risk Management with Linda Sullivan and Steve Young
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Michael Poku, MD, MBA: Improving Minority Representation in Clinical Trials
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Dana Deighton: Esophageal Cancer Patient and Persistent Activist For Her Own Survival
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Striving for Reliability: Optimizing Patient Report Data through World-Class Design Management with Linda Sullivan, Nat Katz, and Art Morales
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The Upside of Centralized Monitoring During a Pandemic: Linda Sullivan, Duncan Hall, and Rachel Oakley on Optimizing Clinical Trials through Innovative RBQM Technology
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Get Rid of Those Silos: Linda Sullivan, Artem Andrianov, and Johann Proeve on How To Optimize Clinical Trials through RBQM
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Gregory L. Hall, MD: Writing the Book on Health Disparities in African Americans
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Turning Insights Into Action: Linda Sullivan and Ken Getz on How Metrics and Benchmarking Provide a Path To Optimizing Clinical Trials
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Lisa Carlton, PhD: Fighting Rare Diseases as a Mother, Patient Advocate and Regulatory Affairs Professional
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Peter A. DiBiaso, MHA: Taking on the Ironman, Mount Kilimanjaro and Parkinson’s disease: a clinical trials patient recruitment expert speaks about his own life as a patient
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Now Is the Time: Making Your Clinical Trial More Resilient
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Hong Liu, PhD, Making Chicago a Healthier City for Asian Americans
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Roslyn Daniels, Black Health Matters Founder and President, on Health Disparities and Exciting Communities About Health
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Dorelia Rivera: Health Disparities, a Career in Advocacy, and Saving Her Daughter’s Life
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Christopher Gantz, Building Trust and minority enrollment in clinical trials at Thomas Jefferson Hospital in Philadelphia
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Communicating the Value of Clinical Trials to Underserved Minority Communities
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People, Process and Technology: The Right Combination for Successful Expert Committees
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Bringing Clinical Trials Closer to Home: Smaller, Local Sites Build Trust & Provide Access to Local Communities
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Raise Your Voices: Social Network Provides Safe Place for Patients to Share Stories and Influence Research
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Brian Loew, The INSPIRE social network platform provides a safe place for patients to meet, learn, and influence research
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Frank Sasinowski, MS, MPH, JD Hymen Phelps & McNamara: Rare Disease Regulatory Transformation: 1983 AIDS Crisis to Present
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Thomas Farrington: Cancer Survivor’s Prostate Health Network gets African American Communities Talking About Prostate Cancer
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We Should Not Be Surprised: COVID-19 Disparities Lay Bare What’s Been There All Along
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COVID-19 Doesn’t Play Fair: What We Need to Understand About Racial Disparities
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Dr. David Fajgenbaum, MD, Castleman’s Disease Survivor, Facing COVID-19 with Research, Action, and Hope
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Turning Passion Into a Career: Insights from a Physician and Industry Medical Director of AbbVie Pharmaceuticals, Charlotte Owens, MD, FACOG
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An Inside Look at the Role of Data Monitoring Committees with Dr. Jonathan Seltzer
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Biostatistics and Biomarkers for the Reliability and Efficiency of Clinical Trials: A Conversation with Dr. Janet Wittes
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An Interview with Dr. Jeffrey Cooper: Clinical Trial Expert and Participant
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Julia Jenkins, EveryLife Foundation for Rare Diseases: Patient’s shape science-driven public policy
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Ensuring Genetic Counseling is Incorporated Into the Patient Experience: An Interview with Sarah Zentack & Leslie Urdaneta
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An Inside Look at Angelman Syndrome Rare Disease: An Interview with Amanda Moore
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Blazing New Trails in Rare Disease & CNS Clinical Studies: An Interview with Dr. Mark Opler
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Developing Novel Treatments for Rare Disorders: A Look at MPS I with Dr. Emil Kakkis
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Learning How to See Differently: An Interview with Kristin Smedley, President of the Curing Retinal Blindness Foundation
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Mark Dant, Pushing for Research that Saved His Son’s Life in the Fight Against MPS I
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Sarah Tompkins, on Having Ehlers-Danlos Syndrome, Having a Mis-Understood Disease, and Taking a Lead in Advocacy
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The Role and Importance of Genetic Counselors to Patients: An Interview with Karmen Trzupek of InformedDNA
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Chasing My Cure: an Interview with Dr. Fajgenbaum
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The State of Clinical Trials in Autism and Neurodevelopmental Disorders with Dr. Scott Hunter
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The New Paradigm of Patient Recruitment: an interview with Mark Summers
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Exciting Developments in Psychopharmacology with guest Andrew Cutler, MD
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The Role of Expert Committees in Clinical Research with guest Jonathan Seltzer, MD, MBA, MA, FACC
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The Most Pressing Challenges and Opportunities in Pain Research with guest Nathaniel Katz, MD, MS
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Important Trends in CNS Clinical Trials with guest Cristoph Correll, MD
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The Most Pressing Challenges in Psychiatry Clinical Trials with Leslie Citrome, MD, MPH
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