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Kader Gedik, MD

Physician-scientist and pediatric rheumatologist with expertise in rare and complex immune-mediated, autoimmune, and autoinflammatory diseases, as well as translational immunology. Former NIH Associate Investigator with over a decade of clinical rheumatology experience spanning patient care, clinical research, and translational science. Draws on leadership roles in NIH-funded translational research, investigator-led studies, and international multidisciplinary collaborations to support the development of innovative autoimmune therapies.

• Read: Case Study: Managing Complexity in an Autologous Cell Therapy Trial

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  Sep 22, ‘26 | 8 min read

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• Read: How Investigator Engagement Builds Enrollment Momentum

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  How Investigator Engagement Builds Enrollment Momentum

  Sep 21, ‘26 | 6 min read

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    Lisa Lopez

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• Read: Case Study: Nectin 4 Biomarker Testing for Oncology Clinical Programs

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  Case Study: Nectin 4 Biomarker Testing for Oncology Clinical Programs

  Sep 14, ‘26 | 3 min read

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    Christie Bongel

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• Read: Has the rest of the world finally caught up with Latin America?

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  Has the rest of the world finally caught up with Latin America?

  Sep 02, ‘26 | 5 min read

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    Andrés Bayona

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• Read: Case Study: Rapid Execution of Assay Validation Rescued Global Study

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  Case Study: Rapid Execution of Assay Validation Rescued Global Study

  Aug 20, ‘26 | 7 min read

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  • Christie B.

    Kennon D.

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• Read: Clinical AI at Scale: Why Trust Matters More Than Speed

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  Aug 18, ‘26 | 6 min read

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• Read: Hidden Strategic Edge in Clinical Trials: Financial Project Management

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  Hidden Strategic Edge in Clinical Trials: Financial Project Management

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    Romy Kane

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• Read: Why Most Early Autoimmune Trials Fail to Yield Decision-ready Evidence

  Early Phase Research - Autoimmune

  Why Most Early Autoimmune Trials Fail to Yield Decision-ready Evidence

  Aug 10, ‘26 | 6 min read

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    Rui F Duarte-Lopes

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• Read: Why Global Oncology Evidence May Not Support U.S. Regulatory Approval

  Clinical Trials - Regulatory

  Why Global Oncology Evidence May Not Support U.S. Regulatory Approval

  Aug 03, ‘26 | 9 min read

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    Harpreet Singh, MD

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