RAPID SITE READINESS
Beginning January 2024, ICE Global will offer Site Readiness services with the aim of reducing site start-up times & shedding unnecessary administrative burdens from the Sponsor, CROs and most importantly, Sites!
APPROACH
ICE Global drives the effort for collection of critical initial documentation required for site activation. Post-activation, we work collaboratively with Sponsor, CRO, CRA and Sites on secondary, lower risk documentation collection. This two-phase approach allows for minimum up-front criteria for Site documentation sign-off and condenses overall site activation timelines. Sites are ready for the final clinical components more rapidly than historical timelines, relieving both Site and Sponsor/CRO frustrations.
ROBUST SITE SUPPORT
ICE Global provides 1:1 Site support in document and ethics preparations to streamline the activation process and reduce timelines. By partnering with Sites to activate earlier, the needle is moved forward on screening and enrollment. This approach ensures accurate site activity projections, and supports competitive enrollment which, in turn, leads to reduced site-related costs.
About Maria:
Maria specializes in site activation and various supporting aspects of clinical operations with 17+ years of industry experience. An avid champion of clinical research sites, Maria believes sites are the backbone of clinical research; her methods are designed around working with sites as unique entities versus a one-size-fits-all approach.