Budget Negotiation 101
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Institution
Onboarding & Training for Clinical Research Professionals
In this webinar, Miranda Schramm, Director of Training at Advarra, covers strategies for new hires joining the clinical trial industry.
Didn’t Expect That to Happen: Events That Must be Reported Promptly to the IRB
Learn what events need to be reported to the IRB after study approval and explore scenarios to help evaluate potentially reportable events.
Increasing Diversity, Equity, and Access in Clinical Research: A Case Study
In the evolving landscape of clinical research, increasing diversity, equity, and access has become a pressing priority. A Clinical
Diversity and Inclusion: Who is Responsible – Site, CRO or Sponsor?
Diversity and Inclusion: Who is Responsible – Site, CRO or Sponsor? Attaining a diverse trial patient population is crucial to
Clinical Research in the COVID-19 Era: Methods for Continuity
The COVID-19 pandemic has led to a significant shift in day-to-day research operations. To keep research moving forward, sponsors need to build a solid foundation to support the virtualization of key components of clinical trials. In addition, the industry needs to maintain a participant-centric approach while ensuring participant safety and regulatory compliance throughout the trial.
EVAL Case Study with Case Comprehensive Cancer Center
Discover how the Case Comprehensive Cancer Center used Advarra EVAL to streamline CCSG workflows, improve data analysis, and show research ROI.