Case Study: Cedars-Sinai Samuel Oschin Comprehensive Cancer Institute achieves faster clinical trial enrollment and streamlined consent with DocuSign

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Cedars-Sinai Samuel Oschin Comprehensive Cancer Institute, where an experienced research manager leads clinical trial efforts, faced a persistent enrollment problem: only 3–5% of adult cancer patients join trials and about 85% are unaware of relevant studies. That low participation is worsened by burdensome paper-based consent, regulatory and funding paperwork that slows study openings and patient enrollment.

The institute replaced paper processes with a DocuSign-powered digital registry for the Research for Her program, enabling mobile access, faster electronic consent and more secure recordkeeping. The change cut document turnaround from three–four weeks to as little as two days, reduced administrative burden so coordinators spend more time with patients, and accelerated study start-up and funding sign-offs.


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