Our protocol-trained, central study coordinators can work on multiple, delegated tasks to free up valuable time of on-site coordinators. As a result, on-site study coordinators can focus on participant recruitment and visits. Central study coordinators can perform phone recruitment, EDC entries, data quality control, facilitate scheduling, send HIPAA compliant SMS reminders to patients.
We can perform and manage EDC entries with our central coordinators and conduct quality assurance for site eSource documents. With centralized EDC entries, CROs and sponsor only need to contact KCRS for all EDC queries.
We can provide protocol design, writing, and amendment. We have staff with more than 50 years of combined experience in conducting FDA regulated studies.
We can create online central campaigns for clinical trials using social media. With our capabilities to access and manage CTMS centrally, we can direct marketing leads directly to the site’s CTMS for timely recruitment follow-up.
We can develop protocol-specific apps to assist busy clinicians and investigators identify, refer or recruit participants.