ACRP Fellow David J. Morin, MD, FACP, CPI, FACRP, reflects on how bringing stakeholders together around a shared purpose can reduce inefficiencies, improve collaboration, and help clinical research better serve patients.
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I first became a CRC in 2004, and I love my job. But there is a part of being a CRC that no one talks about enough: the mental weight of always having so much in motion.
For clinical research sites, manual data entry remains a substantial burden that drains resources and increases study timelines. This impact is worsening as clinical trials become increasingly complex, with more endpoints, procedures, inclusion/exclusion criteria, and data sources.
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