Protocol calendars drive a wide array of study-related activity for teams throughout your organization. To keep your study startup processes on track and ensure quality calendars, it’s important to optimize your calendar-building staff and your processes.
Learn the qualities of an ideal CRA and the necessary competencies for success in the clinical research industry.
Expert webinar presenter answer attendee questions about the tool she developed to assess clinical trial staff workloads.
Expert webinar presenter answers attendee questions about strategies for effective project management of clinical trial workloads.
During this webinar, Forte’s Director of Analytics, Wendy Tate, outlines essential factors of effective clinical trial project management and provides tips to help you successfully manage your individual research portfolio.
Delayed study start-up is a chronic problem in the research industry. This infographic explores steps for clinical research sites and sponsors to improve relationships and speed up study activation timelines.
How well do you know your clinical research abbreviations? Here’s a cheat sheet to some common acronyms and abbreviations that you might encounter.
During this webinar, Christina Brennan of Northwell Health discusses the benefits of centralizing research operations by establishing a central clinical trials office.
Creating processes that result in accurate, timely and complete data are invaluable when implementing or optimizing a CTMS. Here are a few tips to achieve your goals.
Use these tips to streamline training workflows for protocol staff at your organization.