In clinical trials, studies are complex, time-intensive and leave little to no room for error. Particularly when conducting concurrent studies with limited resources, it can be difficult to ensure quality and timely data collection *and entry on every study. This can lead to stress and unhappiness with staff despite the meaningful work they contribute to improve treatment options. Clear and effective project management can make or break the success of a clinical trial, and project planning and management are a key part of achieving quality clinical data
*Please Note: This is a replay of a webinar from the ACRP Global Conference
The presenter is Vatche Bartekian, President, Vantage Bio Trials
If you are interested in registering for this event please e-mail Laurie Burnside at email@example.com.Click here to purchase contact hour.