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The StrokeNet Clinical Research Professional (CRP) Mentoring Program is designed to support the professional growth and development of clinical research personnel at all career stages. The program connects new and experienced research professionals throughout the network with leaders in StrokeNet to foster meaningful mentorship relationships, enhance clinical research skills, and strengthen our research community.
Interactive session focused on communication best practices, where mentees will share their experiences and discuss effective communication with providers, staff, patients, and families.<br>Mentor: Heena Olalde
60 min · 5 slotsThis Jeopardy themed game was created to help CRPs understand and apply consent rules across different scenarios and regulatory contexts. The game features categories like regular consent, LAR consent, and non-English consent, with varying difficulty levels and both scenario-based questions and knowledge questions.<br>Mentors: Andrea Escobar & Macy Barrios
60 min · 5 slotsMentor reviews stroke imaging basics (parenchymal / vascular / perfusion) and function of the imaging Core Lab.<br>Mentor: Vivek Khandwala
60 min · 5 slotsReview of StrokeNet Good Clinical Practice Standard Operating Procedures with imbedded questions throughout. Session is designed for study team members with experience working on a StrokeNet trial.<br>Mentor: Cristina Francois
120 min · 10 slotsIn this session, mentees bring their StrokeNet Informed Consent Documents they would like to practice with a mentor or peer. Mentors will provide feedback and other best practice including teach back and testing participant comprehension.<br>Mentors: Christina Mihova, Josette Elysée, Sue Roll, and Jessica Staloch
90 min · 5 slotsReview of trial site selection, CTA, RA, Regulatory Packet, Start-up Expectations, WebDCU Regulatory Database (DOA, Site & People Documents), Readiness Call.<br>Mentors: Jenn Golan & Heena Olalde
60 min · 10 slotsDesigned for research professionals working on StrokeNet trial start-ups, and those who would like to learn more about the reliance process and requirements, differences between a central and local HRPP. Mentors will review the difference between a central IRB and the local IRB, HRPP vs. IRB, StrokeNet "in-network" sites vs. "out-of-network" sites, and FWAs.<br>Mentors: Sue Roll and Kinga Aitken
90 min · 5 slotsMentors review data management practices in WebDCU using real-world scenarios to identify common errors and improvement strategies. Designed for new coordinators with WebDCU access.<br>Mentor: Jocelyn Craven
60 min · 5 slotsReview of StrokeNet structure and function of different cores / groups. Where to find tools and training resources.<br>Mentors: Laura Benken & Iris Davis
60 min · 5 slotsInteractive role-play where mentees are in the REDCap eConsent "driver's seat" while mentors and provide coaching. Practice remote eConsent, troubleshoot common issues, access completed eConsent files for WebDCU upload, and build confidence using REDCap eConsent best practices.<br>Mentors: Abbey Staugaitis & Anthony Rogers
60 min · 1 slotsMentors review how to best prepare for a monitoring visit.<br>Mentor: Jama Olsen
60 min · 5 slotsMentor walks through pharmacy responsibilities at Clinical Performing Sites for drug dispensing, inventory, temperature excursions, and regulatory requirements. Designed for anyone with WebDCU access on a StrokeNet Research Pharmacy supported trial. (ASPIRE, CAPTIVA, FASTEST, SISTER).<br>Mentor: Brittany Dornheggen
60 min · 5 slots