Three protocol calendar building strategies for your clinical research site to consider.
Learn how recent changes to CCSG guidelines affect how cancer centers demonstrate their impact.
Here we reveal why waiting until you have a full study pipeline to purchase a CTMS can be a drawback to the success of a system at your research site. Learn why you should consider purchasing even while your study pipeline is small.
Dr. Wendy Tate discusses the industry’s progress toward greater inclusivity in clinical trials and identifies the continued need for improved diversity in research.
The initiative will co-develop and publish a standard data dictionary and API definitions for patient/trial matching and recruitment technologies.
Following her recent presentation on the clinical research components of the NCI Cancer Center Support Grant, Regina Schwind answers attendee questions.
Analyzing your organization’s strengths can help you validate your current clinical research operations, but uncovering your weaknesses will drive you towards true growth.
Co-presenter, Beth Harper of Clinical Performance Partners, addresses attendee questions following Forte’s recent webinar on advertising clinical trials for patient recruitment.
Learn how to find the right individual to manage your clinical research projects and improve the efficiency of your clinical trials.
Creating feasibility assessments can be as frustrating for sponsors as answering questionnaires is for sites. Here’s how sponsors can alleviate these frustrations, according to sites.