Newsletter | October 26, 2026

10.26.26 -- Participant Payment — Make It Make Cents

SPONSOR

Why next-generation ADC trials demand real-time visibility

The success of next-generation ADC trials depends on more than breakthrough science. Sponsors must navigate increasing operational complexity while protecting patient safety and maintaining study momentum. Learn how leading organizations are using proactive risk management, real-time clinical oversight and connected data platforms to accelerate decisions, reduce delays and improve the patient experience. Explore real-time ADC trial strategies.

CLINICAL SITES

5 Sponsor Contracting Issues That Delay Clinical Trials — And How To Avoid Them

CTA negotiations don’t have to stall study start-up. Learn five sponsor-side contracting issues that cause delays and practical ways to prevent them.

Who Owns The Work Behind Clinical Trial Complexity?

Site burden often points to unclear ownership. This article examines how recurring administrative work reaches sites, where standardization helps, and when responsibility should shift.

Psychedelic Drug Trials: Are Your Sites Ready?

Psychedelic trials require unique operational approaches. Learn how to address patient safety, blinding, specialized assessments, and therapeutic setting considerations.

PATIENT CENTRICITY

Participant Payment — Make It Make Cents

Participant payment practices and expectations vary wildly. With advocate T.J. Sharpe, explore why sponsors need to rethink how they appreciate participants' time, effort, and burden.

When Patient Burden Becomes A Retention Risk

Patient burden is not theoretical. In this clip, we hear professional insight into why sponsors need to understand patient burden before a trial is underway.

Leading Rare Disease Research

Rare disease trials demand specialized expertise. Learn how patient- and site-focused strategies can reduce burden, strengthen recruitment and retention, and support trial success.

PATIENT RECRUITMENT

Can A Universal Health Screening Help Stop Clinical Trial Dropouts?

Could comprehensive health scans give trial participants meaningful value — and help sponsors reduce costly dropouts?

Why Are Sponsors Prioritizing Ophthalmology Clinical Trials?

Explore how demographic shifts and retinal innovation are transforming ophthalmology trials, and why operational precision is the key to protecting data integrity in this high-growth sector.

The Evolution Of GLP-1s: Overcoming Clinical Development Challenges

Explore clinical development trends, recruitment hurdles, study design strategies, and emerging therapies shaping obesity and metabolic disease research.

Removing Barriers To Trial Participation

Learn how one platform is transforming the participant journey to deliver a 60% reduction in participant drop-out and 97% engagement rates, improving retention for even the most vulnerable populations worldwide.

Solutions For Patients Across Most Therapeutic Areas And Indications

Struggling with slow recruitment or fragmented sites? Explore how 35 coordinated sites and 3.5M+ patients can streamline trials from startup to close.

From Weeks To Days: An Innovative Approach To Patient Recruitment

Discover how AI-driven, personalized communication can break linguistic and literacy barriers to make patient recruitment faster, more inclusive, and 30% more effective.

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