This comprehensive workshop provides compliance professionals with an in-depth understanding of the critical roles and responsibilities IRB administrators hold throughout the entire life cycle of a research protocol. From the initial submission of a new research protocol to its final study closeout, this workshop equips participants with the tools and knowledge needed to navigate the complexities of protocol management and regulatory compliance.
Delivered in three interactive 2-hour sessions, the workshop is designed for IRB administrators and research compliance professionals. It focuses on the challenges and nuances of managing protocol reviews within highly regulated environments, providing hands-on experience to address key issues that arise in both early-stage and late research.
Through practical activities and collaborative discussions, participants will apply core concepts and strategies to real-world scenarios, strengthening their ability to manage research protocols effectively while ensuring compliance with regulatory guidelines and ethical standards.
This workshop is ideal for professionals who interact with the IRB process including clinical coordinators, clinical research associates, and monitors or anyone involved in managing and submitting protocols. It offers valuable insights into the regulatory landscape and practical solutions to optimize your workflow, ensuring that protocols are managed effectively and are compliant.