Clinical research does not end when a protocol is executed, data are cleaned, or a study report is complete. This session introduces medical communications as a practical, cross-functional bridge between clinical operations, evidence generation, technology platforms, and the patients and professionals the research is meant to serve. Using real-world, noncommercial examples, attendees will examine how study teams can plan for evidence translation earlier in the research lifecycle, connect trial execution decisions to downstream communication needs, and use integrated tools and workflows to improve clarity, consistency, and reach.

Panelists for this session will emphasize how attendees can partner with colleagues from other realms of stakeholders in the research to craft effective communications without compromising scientific rigor, compliance, or operational quality. Attendees will leave with a replicable framework for turning well-run research into credible, accessible, and actionable evidence.

CEU: 1.0 ACRP

Speakers:

• Maureen Jahraus, BS, MBA, Global Head, Medical Communications, Resmed

• Fatima Sert, PhD, Director Clinical Research, Americas, Resmed