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All CRIO Company News Running a Site Running a Study Recruitment & Diversity CRIO Culture
Running a Site 1 Minute Read

Clinical Research IO’s Survey Finds That Coronavirus is Disrupting Clinical Research Sites

Clinical Research IO‘s recent web survey found that COVID-19 is disrupting clinical research sites worldwide. The results are indicative of a significant slowdown in new drug development and long term effects on healthcare in general. 25% of sites have stopped recruiting Of the 75% that are continuing enrollment, about half (37%) are considering halting new...

Running a Site
3 Minute Read -

Clinical Trial Site Workload is increasing, but Budgets are Shrinking During Coronavirus

In early March 2020, Clinical Research IO conducted a clinical trial industry survey and found that COVID-19 is disrupting clinical research operations at all 73 participating sites. As the situation continues to evolve, sites are forced to constantly adapt. The majority have halted new patient enrollment for ongoing studies but will continue to conduct visits...

Running a Site
1 Minute Read -

The Clinical Trial Business Development Lifecycle

Webinar Date: February 17, 2020 Webinar Guests: Mark Ragusa, former Director of Research at Raleigh Neurology Associates Don’t do clinical trial business development haphazardly. Mark Ragusa, former Director of Research at Raleigh Neurology, shares his framework for systematically targeting and nurturing your sponsor and CRO relationships to create a rich, site-appropriate study pipeline. Raleigh Neurology...

clinical-research-coordinator-interview-questions
Running a Site
6 Minute Read -

10 Questions You Should Ask When Interviewing a Clinical Research Coordinator

Hire your dream Clinical Research Coordinator. Reveal your applicant’s true capabilities with these 10 questions. When I interviewed for my first coordinator job, I was left alone in a back-office waiting for at least 45 minutes before the Prime Coordinator remembered I was there. She rushed out of the room to collect her materials and...

electronic-source-e-regulatory-clinical-trials
Running a Site
4 Minute Read -

The Coming Wave of Electronic Source (eSource) and eRegulatory for Clinical Trial Sites: Survey Insights

See exclusive survey data on what technologies clinical research sites are currently using, how much they’re spending, and why Electronic Source (eSource) and eRegulatory software is poised to break out in the clinical trials industry. Motivation for eSource and eRegulatory Survey Clinical Research IO (CRIO) was founded on the belief that we can get life-altering...

The Real Reason Sites Need eSource
Running a Site
12 Minute Read -

The Real Reason Sites Need eSource

Most discussion about electronic source (eSource) documentation in the clinical research enterprise starts from a sponsor standpoint, with eSource being viewed as an extension-almost a mobile version of electronic data capture (EDC). In this view, sponsors provide sites with eSource systems that the sites use to collect data, which are then transmitted to the EDC...

Running a Site 1 Minute Read

eSource In The Age Of Complexity

When a study coordinator uses eSource, he or she enters data into an electronic system like an electronic medical record or tablet computer, rather than onto paper. Data can then be transferred from the eSource system into the electronic case report (eCRF) system (also known as the electronic data capture (EDC) system), thus eliminating the...

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