Summit: Participant Recruitment
This course describes methods for building trust with participants who are a “good fit” for the clinical trial. The course explains the importance of IRB-approved...
Read The ArticleThis course describes methods for building trust with participants who are a “good fit” for the clinical trial. The course explains the importance of IRB-approved...
Read The ArticleA foundational course for individuals considering a career as a clinical research associate (CRA). The course provides broad training on the ethical, regulatory, and practical...
Read The ArticleJust ASK™: Introduction to Equity and Diversity in Clinical Research and Trial Participation is designed to provide learners with a foundational understanding of equity, diversity,...
Read The ArticleThe data people generate by interacting with digital systems, such as smart devices, phones, and online platforms, have become a gold mine for research. Researchers...
Read The ArticleThis in-depth course provides practical knowledge on how to develop, negotiate, and implement a clinical trial budget from the perspective of the clinical site. It...
Read The ArticleThis course prepares medically trained individuals to become new medical monitors and enhances the knowledge of current medical monitors. Medical monitors participate as team members...
Read The ArticleLeadership is an integral part of career development for individuals across professions and disciplines. This course introduces critical areas of leadership, including communication, relationship building...
Read The ArticleThis course provides the basic concepts of what clinical research is, how it is carried out and by whom, and its underlying ethical and regulatory...
Read The ArticleThis webinar introduces a scalable model for establishing a research coordinator float pool to support clinical research operations across institutions. Using Johns Hopkins’ RCSS model...
Read The ArticleIND safety reporting is a core function of clinical trials. Study sites and sponsors are responsible for reporting adverse events (AEs), serious adverse events (SAEs),...
Read The Article