While bugs are as natural in coding as they are in nature, we don’t want them creeping into our code. At CRIO, we have established various processes and procedures to handle bugs. At the close of 2022, we hosted a Bugathon, part of our ongoing efforts to deliver best-in-class quality. The Bugathon was a two...
Overview With 9 locations in Texas, California and Louisiana, Benchmark Research is the world’s leading vaccine network. Benchmark has performed over 10,000 studies on over 40,000 subjects and has received numerous awards, including being a five-time recipient of the Best Clinical Trial Site/Network award from the World Vaccine Congress. Challenge Historically, Benchmark used paper charts...
With the recent push toward Decentralized Clinical Trials (DCTs), many sponsors are adopting eConsent. eConsent allows patients to consent electronically, whether in clinic or remotely, from the convenience of their home. eConsent offers sponsors, CROs, investigators and patients these benefits: Reduce errors by ensuring completion of all fields Automated audit trails ensure accuracy of date-times...
BOSTON, MA – August 9, 2022 – CRIO, a Boston-based healthcare technology company streamlining clinical trials for sponsors, sites and patients, announced that it has reached another milestone, exceeding 2,000 clinical research sites standardizing on CRIO’s eSource platform. CRIO supports a variety of clinical trial data. To date, over 800 life science sponsors have data...
Clinical research coordinators (CRCs) shoulder significant responsibility in the conduct of clinical trials — seeing back-to-back patients, processing labs, completing data entry, responding to emails, liaising with monitors — and play an incredibly important part in the research process. As clinical trial complexity increases and more emphasis is placed on data quality, the demand for...
Dr. James Clark of Charlottesville Medical Research recently had an FDA inspection of his site as it is a high enroller. He did not receive a FDA Form 483, and he was using the CRIO electronic source system on the study. Learn about his experience in this Q&A session. CRIO: What’s your background? Dr. Clark:...
Between loads of emails and back-to-back patients, the clinical research super-coordinator swiftly and accurately manages your site’s data collection, leaving you with peace of mind at the end of a long day. One can only imagine what might happen without a super-coordinator by your side…the horror! Unfortunately, it’s more common than many site owners would...
With trial activities ramping up at both the site and sponsor levels, it is inevitable that the amount of work for sites will increase. In preparation, sites should start thinking about how to bring back site staff and how work should be distributed amongst them. One great option that sites can consider is developing a...
At Clinical Research IO we work with thousands of clinical research professionals, such as clinical research coordinators, each day. As a CRIO Project Manager, I am fortunate enough to have the opportunity to develop one-on-one relationships with my clients — relationships that are more than just your typical software vendor-customer contracts. I spend a lot of...
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...
