patient-centric trial

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Clincierge Voice of the Patient Study Cited in Xtalks Webinar Press Release

Press Releases / By

Xtalks is the world’s leading provider of educational webinars for the international life sciences community. They recently cited statistics from our Voice of the Patient research study in a press release for an upcoming webinar. The webinar, entitled Unlocking Patient Engagement: Enhancing the Clinical Trial Experience with Consumerization, discusses the essential technologies, features, and processes …

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CISCRP Diversity Ad Spring 2023

CISCRP: Supporting Patient Diversity Campaign 2023

Media Coverage / By

Clincierge is proud to support CISCRP in a new educational initiative to increase awareness about clinical research and the level of understanding among minority communities across the U.S.We have united to circulate an informative full-page advertorial spread highlighting the key importance of diversity in clinical studies to discover treatments that are effective for everyone.

Health Equity and DEI: Are They Synonymous?

Health Equity and DEI: Are They Synonymous?

Diversity, Education / By

Due to a lack of health equity and many existing health disparities for rare disease patients, their access to clinical trial participation is often greatly diminished. With limited education and finances, many do not know about trial opportunities, while others cannot fathom the additional costs of participating.

Drug discovery predictions: Analysis and insight

Drug Discovery Predictions: Analysis and Insight

Media Coverage / By

In this Drug Discovery World article, author Megan Thomas spoke with decision makers from the clinical trial industry, including Clincierge’s CEO, Scott Gray, about their predictions on what 2022 holds for our sector, including the importance of patient-centricity and improved stakeholder engagement in clinical trials.

CISCRP Patient Diversity Campaign

CISCRP: Supporting Patient Diversity Campaign 2022

Media Coverage / By

Clincierge is proud to support CISCRP in a new educational initiative to increase awareness about clinical research and the level of understanding among minority communities across the U.S.We have united to circulate an informative full-page advertorial spread highlighting the key importance of diversity in clinical studies to discover treatments that are effective for everyone.

SCRS_INSITE_AMPLIFYING_THE_VOICE_OF_THE_PATIENT_IN_RARE_DISEASE_TRIALS

Amplifying the Voice of the Patient in Rare Disease Trials

Media Coverage / By

Featured in SCRS InSite Journal: Scott Gray, CEO, discusses patient recruitment and retention, two of the most pressing challenges facing clinical research today. Continue reading to learn more about understanding the financial, logistical, and emotional barriers to participation, the consequences of poor retention and enrollment, actionable steps to improve trial outcomes, and other key findings …

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Voice of the Patient Research

View the results of our recent research to explore how effective patient support strategies can reduce barriers, increase retention, and improve outcomes in rare disease clinical trials in our latest eBook.

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Voice of the patient