The Clinical Research Team at BRANY is responsible for overseeing the ethical and regulatory aspects of clinical trials. They manage Institutional Review Board (IRB) processes, ensuring compliance with Good Clinical Practice (GCP) and conducting audits to maintain high standards. The team coordinates study start-up activities, facilitates communication between stakeholders, and provides support for adverse event reporting, ultimately ensuring that clinical research is conducted safely and ethically.
Hila Kalavres
IRB Meeting Specialist
Jill Filipelli
Operations Manager, Clinical T...
Jorquera Erika
Associate IRB Coordinator
Leah Beth Persky
Clinical Research Compliance A...
Liz Garger
Project Specialist
Mbms Monalia Smith
Junior Associate IRB Coordinat...
Olga Pizov
GCP Auditor And Monitor
Raffaella Hart
Senior Vp, Irb, Ibc, And QA Se...
Sujen Rashid
Junior IRB Coordinator
Ted Armbruster
IRB Coordinator
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