by Neeli Sharrett | Dec 5, 2020 | News & Insights
Dec 05, 2020 – 2020 has been a challenging year. There has been a lot of uncertainty, misinformation, and fear. We have, like most of you, been operating in a mostly-virtual existence since March to limit the spread of COVID-19. Heading into the fall with cases...
by Neeli Sharrett | May 8, 2018 | News & Insights, Resources
May 8, 2018 – No sponsor ever intentionally selects a site that will do poorly. No site ever commits to doing a protocol intending at the outset to do a bad job or be non-productive. But everyone knows the substantial costs in terms of time, money, and missed...
by Neeli Sharrett | Mar 12, 2018 | News & Insights, Resources
March 12, 2018 – You know what you want your study to look like. You have probably done your homework and know what your competitors have tried, what the regulators are expecting/requiring, and you’ve confirmed that you are aligned with current medical practice and...
by Kim Morris | Oct 18, 2017 | News & Insights, Resources
October 18, 2017 – Ellie Einolhayat, RN, a Lexitas monitor (clinical research associate) provides insight on the role onsite monitors have in identifying issues with protocol design and other challenges that come with successfully executing a clinical trial. To learn...
by Kim Morris | Sep 22, 2017 | News & Insights
Chad Ice, CEO of Lexitas, discussed the company’s extensive experience in clinical trials. Mr. Ice shares details of who Lexitas is, their expertise in Ophthalmics as well as keen focus on delivering exceptional service to their sponsors. Damien Goldberg, MD also...
by Kim Morris | Sep 5, 2017 | News & Insights
If you are in the clinical research business (and presumably you are if you’re reading this!), you understand the role of a clinical research associate (CRA), commonly referred to as a monitor. The primary function of a CRA is to follow Good Clinical Practice to...