Newsletter | July 27, 2026

07.27.26 -- Optimizing The Clinical Lifecycle: Evaluating Site Models, Unlocking Social RWD, And Elevating Representation

SPONSOR

Webinar: Rewriting the Code: Advances and Challenges in Pediatric Gene Therapy

Pediatric gene therapy is rapidly transforming treatment for rare genetic diseases. Join Dr. Rachel Abu Taleb as she explores AAV, lentiviral, and CRISPR platforms, reviews lessons from approved therapies, and examines the scientific, regulatory, and access challenges shaping future innovation. Learn how these advances are redefining care and improving outcomes for children with rare diseases. Click here to learn more.

CLINICAL SITES

How Clinical Research Site Operating Models Perform in Practice

In part two of this three-part series, Paradigm Clinical Research CEO Kurt Mussina evaluates how each site operating model performs regarding speed, patient access, investigator engagement, quality, accountability, and scalability.

Redefining eSource: A Smarter Approach To Clinical Trial Data Capture

Discover how AI-powered extraction and site-centric workflows improve data quality and reduce administrative burdens for research teams.

The Stakeholder Impact of Centralized Trial Services

Real‑world experiences show how centralizing logistics and payments streamlines coordination, reduces site burden, and improves trial execution.

SPONSOR

The evidence gap in Hematology: From trial endpoints to patient outcomes

As hematology trials become more complex, sponsors face increasing pressure to accelerate development while generating stronger evidence, mitigating recruitment risk and supporting faster patient access. Join Parexel's experts to discover how RWD/RWE can help you make smarter decisions earlier, mitigate risk and strengthen your path from development to approval. Don't miss this opportunity — register today.

PATIENT CENTRICITY

Social Media Is Replete With Patient RWD, But How Can Researchers Best Use It?

Pistoia Alliance's Thierry Escudier and Aditya Tyagi discuss how social media listening is used in clinical research, how it supports established evidence-generation methods, and how it can become a credible, structured input for drug development.

The Lasting Impact Of Treatment Gaps In ARG1-D

A patient story from ARG1-D reveals how even brief treatment interruptions can trigger irreversible decline and why continuity of care must remain a priority in rare disease research.

Precision Partnership For Obesity Clinical Trials

Accelerate obesity research with specialized expertise in GLP-1 trials. Our approach ensures rapid enrollment, high participant retention, and clean data through a patient-centered model.

PATIENT RECRUITMENT

Early Patient Education And Community Outreach Are Advancing Representation In Clinical Trials

Merck Executive Director, Clinical Trial Patient Representation, Adrelia Allen argues that patient awareness, access, early information, and trust shape are the pillars of patient representation in clinical trials.

Quantitative ROI With DCTs

Through dedicated staffing, operational oversight, and collaboration with site teams, see how we were able to transform a struggling cardiology study into a revitalized recruitment effort.

Designed Around Your Needs: Let's Accelerate Enrollment Together

CSS offers unmatched depth and breadth in therapeutic expertise, providing full-spectrum, in-house capabilities, positing the organization as a true end-to-end partner in clinical trials.

CHOOSE YOUR OWN ADVENTURE

You're receiving the Monday edition of the Clinical Leader newsletter, focusing on Clinical SitesPatient Centricity, and Patient Recruitment. To make changes to your newsletter selections, update your topic preferences.

  • Clinical Sites | Patient Centricity | Patient Recruitment (Monday)
  • Clinical Trial Technology (Tuesday)
  • Decentralized Trials | Trial Management (Wednesday)
  • Outsourcing Models | Regulatory & Compliance (Thursday)
  • Clinical Data Management & Analytics | Trial Monitoring (Friday)

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