Blog
Now hiring: Office Administrator
Pearl IRB is seeking an Office Administrator to join our team! The Office Administrator will work closely with the leadership team to enhance and develop business processes, assist with project management across the service delivery team and...
Pearl IRB is attending Diversity Alliance for Science West Coast Conference
Diversity Alliance for Science (DA4S) is a non-profit organization that provides a platform to identify, attract, and develop small and/or diverse businesses to drive inclusive procurement practices in corporate, academic, and governmental entities within...
FDA commits to develop guidance for clinical trial stakeholders
The US Food and Drug Administration (FDA) recently made two announcements indicating a commitment to addressing questions about the clinical trial process for clinical trial stakeholders, The National Law Review reports. FDA announced two actions in late...
Pearl IRB’s Robert Seevers will deliver lecture to Purdue University drug discovery class
Robert Seevers, Senior Advisor and Adjunct Board Member at Pearl IRB, has been invited to deliver a lecture at Purdue University this Friday, February 16. Seevers will speak to an MS-level drug discovery class that aims to teach students how to...
Implementation of Common Rule changes delayed: FAQs on the new Common Rule
New Common Rule - FAQ Changes to the Common Rule, the principal rule regulating human subjects research, go into effect on July 19, 2018. A number of Pearl IRB policies and procedures will be updated as a result of the changes to the rule. Please note that...