According to Michele Russell-Einhorn, Chief Compliance Officer at Advarra, most research institutions had taken steps to partially or fully suspend…
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According to Michele Russell-Einhorn, Chief Compliance Officer at Advarra, most research institutions had taken steps to partially or fully suspend…
- Ada Zhu, Content Specialist at Clinical Research IO (CRIO) 7 hours agoIn a 2019 CRIO eBook, “Scaling and Innovating: The Consolidation and Reinvention of Clinical Research Sites,” we explored the emerging…
- Team CRIO 7 hours agoNetworks are brick and mortar businesses, by definition, but their differentiation lies in their ability to incorporate and optimize technology…
- Raymond Nomizu, CEO and Co-Founder of Clinical Research IO (CRIO) 1 day agoThere are plenty of instances where institutional capital goes into a sector, only to fizzle out. Why are we confident…
- Raymond Nomizu, CEO & Co-Founder at Clinical Research IO (CRIO) 2 days agoValuation of site for purchase by site networks As site networks compete with each other to purchase clinical research sites,…
- Raymond Nomizu, CEO & Co-Founder at Clinical Research IO (CRIO) 3 days agoThe daunting task of COVID-19 trials The onset of the COVID-19 pandemic posed a new challenge for sponsors. They needed…
- Ada Zhu, Content Specialist at Clinical Research IO (CRIO) 5 days agoWhile bugs are as natural in coding as they are in nature, we don’t want them creeping into our code.…
- Kristen Bosse, Director of Product Development 6 days agoHire your dream Clinical Research Coordinator. Reveal your applicant’s true capabilities with these 10 questions. When I interviewed for my…
- Anna Krauss, Customer Success at Clinical Research IO 5 years agoAchieving representative enrollment – meaning diversity in race, age, gender and socioeconomic status – in clinical trials is essential to…
- Maxine Lai, Content Associate at Clinical Research IO 2 years agoMost discussion about electronic source (eSource) documentation in the clinical research enterprise starts from a sponsor standpoint, with eSource being…
- Raymond Nomizu, CEO of Clinical Research IO 5 years agoDisclaimer: The examples noted in the following article are all firsthand accounts of the author, but for the purpose of…
- Takoda Roland, CCRA, CCRP, CNA, Founder of Philadelphia Pharmaceutical Research 3 years agoHear what it feels like to endure an FDA audit as a Principal Investigator or clinical research site owner, based…
- Bob Bedetti, Business Development at Clinical Research IO 3 years agoElectronic Source (eSource) and Electronic Data Capture (EDC) are increasingly popular technologies for collecting and managing clinical trial data. The…
- Phoebe Stoye, Product Manager at Clinical Research IO 3 years agoYour study doesn't stop just because you're out of town or not in a clinic.
Schedule a Demo or call us at 617-302-9845From the lifecycle of a remote clinical trial, to effective feasibility and planning, patient recruitment, regulatory compliance, and continuity of operations, this is one energetic and spirited conversation you won’t want to miss.
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