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WCG Podcast Library

Explore episodes of WCG’s podcast series, where we interview leaders from across the clinical research and patient advocacy ecosystem.

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Podcast

Dr. David Fajgenbaum, MD, Castleman’s Disease Survivor, Facing COVID-19 with Research, Action, and Hope

Read More about Dr. David Fajgenbaum, MD, Castleman’s Disease Survivor, Facing COVID-19 with Research, Action, and Hope
Podcast

Charlotte Owens, MD, FACOG: Turning Passion Into a Career: Insights from a Physician and Industry Medical Director of AbbVie Pharmaceuticals

Read More about Charlotte Owens, MD, FACOG: Turning Passion Into a Career: Insights from a Physician and Industry Medical Director of AbbVie Pharmaceuticals
Podcast

An Inside Look at the Role of Data Monitoring Committees with Dr. Jonathan Seltzer

Read More about An Inside Look at the Role of Data Monitoring Committees with Dr. Jonathan Seltzer
Podcast

Biostatistics and Biomarkers for the Reliability and Efficiency of Clinical Trials: A Conversation with Dr. Janet Wittes

Read More about Biostatistics and Biomarkers for the Reliability and Efficiency of Clinical Trials: A Conversation with Dr. Janet Wittes
Podcast

Dr. Jeffrey Cooper, MD, living with Parkinsons, and expert in clinical trials, on how hard it can be for patients to find clinical trials

Read More about Dr. Jeffrey Cooper, MD, living with Parkinsons, and expert in clinical trials, on how hard it can be for patients to find clinical trials
Podcast

Julia Jenkins, EveryLife Foundation for Rare Diseases: Patient’s shape science-driven public policy

Read More about Julia Jenkins, EveryLife Foundation for Rare Diseases: Patient’s shape science-driven public policy
Podcast

Blazing New Trails in Rare Disease & CNS Clinical Studies: An Interview with Dr. Mark Opler

Read More about Blazing New Trails in Rare Disease & CNS Clinical Studies: An Interview with Dr. Mark Opler
Podcast

Mark Dant, pushing for research that saved his son’s life in the fight against MPS I and advocating for change

Read More about Mark Dant, pushing for research that saved his son’s life in the fight against MPS I and advocating for change
Podcast

Dr. Emil Kakkis: Developing Novel Treatments for Rare Disorders and Connecting With Patients as Critical Partners in Research

Read More about Dr. Emil Kakkis: Developing Novel Treatments for Rare Disorders and Connecting With Patients as Critical Partners in Research
Podcast

Sarah Tompkins, on having Ehlers-Danlos Syndrome, having a mis-understood disease, taking a lead in advocacy

Read More about Sarah Tompkins, on having Ehlers-Danlos Syndrome, having a mis-understood disease, taking a lead in advocacy
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