Tailored Support for Research Sites
Advarra offers a full range of specialized services designed to the specific needs of research sites, helping to optimize operations at every stage of the clinical trial lifecycle.
Budget Negotiation and Setup
Accelerate budget negotiations with sponsors and reduce the administrative load on your finance team.
CTMS Study Builds
Ensure compliant and efficient study setup by allowing our experts to handle the build directly in your clinical trial management system (CTMS).
Coverage Analysis
Stay compliant with Medicare billing regulations and streamline your coverage analysis process.
Clinical Research Training
Equip your team with the knowledge and skills to effectively use research technology and stay compliant.
Manual Data Migration
Eliminate time-consuming data migration tasks with our large team that handles manual intervention and ensures data accuracy.
Protocol Calendar Build
Streamline study setup with protocol calendars built directly into your CTMS by Advarra’s specialists, ensuring efficient and compliant study operations.
eSource + EDC Study Design
Optimize study design for eSource and EDC systems to ensure efficient trial setup.
Informed Consent Development
Create clear, compliant informed consent documents to enhance participant understanding.
Research Technology Staffing
Gain access to specialized staffing solutions that provide the technical expertise your site needs to manage and optimize research technologies.
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Why Choose Advarra for Site Enablement?
Advarra’s Site Support Services are designed to help research sites increase operational efficiency, meet regulatory requirements, and ensure successful clinical trial outcomes. By providing expert guidance and relieving administrative pressures, we help sites stay focused on what matters most: delivering high-quality research.