Strategic Enablement Services
For Sites and Institutions
Advarra’s Strategic Enablement Services provide sites and institutions with tailored solutions that enhance productivity, increase compliance, and scale technology to maximize study performance and reach execution goals.
Designed and led by a team of seasoned consultants and enablement specialists, Advarra empowers research sites to accelerate study activation and meet the highest levels of research standards, through services such as targeted assessments, effective policy and protocol development, and reliable staffing resources.
Why Partner with Advarra?
Advarra is an experienced and trusted partner for sites and institutions.
Highly Experienced, Flexible Team
Extensive, hands-on industry experience across research compliance, operations, finance, and technology optimization, coupled with the agility to seamlessly and quickly deploy staffing resources
Specialized Resourcing for Greater Efficiency
Skilled support optimized to the complexity
of their clinical research needs for short- and long-term needs
Deep Expertise in Advarra’s Site Technology
Unparalleled knowledge of site technology for impactful recommendations on how to best maximize technology
Trusted leaders with
decades
of clinical research experience
Team of
1300+
ready to support
Industry-leading technology includes
OnCore, Clinical Conductor, eReg, and eSource
Solutions Aligned to Research Site Needs
Advarra provides end-to-end solutions that are critical to clinical research delivery for research compliance, strategy & operations, finance & billing, and technology optimization.
Advarra’s experts partner with sites and institutions to identify solutions that create a scalable, meaningful, and lasting impact. Our solutions support research sites with opportunities to alleviate administrative pressure, reduce risk, and improve operational efficiency.
Our team works to identify solutions that meet needs, such as:
Study Startup
Expert support for coverage analysis, budget development and negotiation, and Clinical Trial Management System (CTMS) builds that streamline study management and reduce startup timelines
Human Research Protection Program (HRPP)/Institutional Review Board (IRB) Advisory
Gap assessments, policy and procedure development, monitoring and auditing support, and Association for the Accreditation of Human Research Protection Programs, Inc. (AAHRPP) certification guidance to meet the highest standards for quality, ethics, and compliance
Clinical Trials Operational Excellence
Strategies, tools, and processes to accelerate protocol activation, boost enrollment, ensure regulatory compliance, and address gaps in research infrastructure
Research Billing & Finance
Full billing cycle policy and procedure analysis to improve workflows, and resource support to optimize the execution of critical processes such as coverage analysis, budget development and negotiation, pricing, invoicing, and research billing – all to maximize revenue recovery and compliance
Site Technology Optimization & Scaling
Strategic recommendations and technical staffing to support integrations and scale of technology platforms for long-term adoption across the clinical research enterprise
Clinical Trial Auditing & Monitoring
Comprehensive auditing, monitoring, inspection readiness, and training to ensure compliance with protocol requirements and Good Clinical Practice (GCP), and confirm data integrity
Ready to learn more?
Learn more about Advarra’s Strategic Enablement Services for Sites and Institutions
