Conduct
The conduct of a clinical research study involves participant recruitment and management as well as study oversight, maintenance, and reporting.
- Study and visit management
- Global trial oversight and reporting
- Site clinical trial management
- Site staffing
- Clinical data management
Study and Visit Management
Centralize engagement and oversight of site operations while providing intuitive resources for visit guidance, scheduling, and visit calculations to increase compliance.
For sites, a clinical trial management system (CTMS) centralizes the management of protocols, participants, and visits, simplifying study management for site staff and allowing them to focus on the patient.
Sites using Advarra Study Startup decreased protocol deviations by 21% compared to non-users.
Global Trial Oversight and Reporting
Complete global visibility for real-time reporting across all site and patient activities assigned, in-progress, and completed on your trial or across your portfolio.
Site Clinical Trial Management
A CTMS is responsible for managing all operational aspects of a clinical trial, from study startup to closeout. Research sites, site networks, health systems, academic medical centers, and cancer centers use Advarra’s CTMS solutions to centralize information related to protocols, subjects, staff, financials and billing, and much more. A CTMS acts as the hub for research operations, simplifying study conduct and improving visibility throughout a site’s research portfolio.
Site Staffing
Industry surveys indicate 29% of respondents anticipate research staffing shortages. Advarra understands your challenges and can partner with you to deliver customized solutions to fit your unique needs. Engage highly qualified research professionals from R1 universities to fill short- and long-term core team roles both on-site, hybrid, or remotely.
Clinical Data Management
For research sites, data management plays a crucial role in ensuring clinical trial success and accuracy. The process involves collecting, organizing, and managing vast amounts of data generated throughout the trial.
Effective data management is essential to ensure the integrity, quality, and reliability of the clinical data. Advarra’s eSource + EDC platform allows site staff to easily capture and manage data, facilitate remote workflows, and eliminate duplicative processes, all in a 21 CFR Part 11-compliant, integrated system.
“The system has helped us improve our data collection processes and helped to make communication more effective. The different options for building form constraints has helped us to ensure higher data quality.”
Courtney Kennedy, DNP, RN-BC
Manager, Clinical Trials Applications, University of Nebraska Medical Center