QA Q&A Corner: Regulations, Records, and Razzle-Dazzle in Research

Q. Who is responsible for ensuring that a clinical study complies with state and local regulations and requirements? Is this a clinical sponsor/monitor responsibility or a matter for the institutional review board (IRB) to address?

A: The U.S. Food and Drug Administration (FDA) has indicated that all parties involved in managing a study have a […]

Michael Causey, ACRP Editor-In-Chief

Talent Management Tools and Tactics for Today’s Researchers

Barring robots automating all of our jobs anytime soon, human talent management will remain one of the top challenges for leaders at study sites, sponsors, and contract research organizations, and for others in managerial roles in the clinical trial lifecycle for the foreseeable future. For Julie Locke, MBA, CCRA, a former clinical research associate (CRA) […]