The 2020 PCORI Virtual Annual Meeting will offer attendees the learning opportunities and networking that have become synonymous with PCORI's premier event focused on patient-centered, stakeholder-driven research.

The meeting will highlight results from several PCORI-funded studies and explore how the time from research to improved health for patients can be shortened. Attendees will:

• Learn about PCORI's efforts to disseminate research findings
• Network with others
• Examine PCORI’s emphasis on engagement
• Explore participation in developing our research agenda
• Listen to powerful, inspiring keynote speakers

This year's sessions will feature PCORI-funded COVID-19 research, telehealth, and health and healthcare disparities, among other hot topics.

Join PCORI for this free event as they celebrate their 10-year anniversary and discuss how, together, researchers can be ready to answer the research questions of the future.

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Join the NRP for a panel discussion on adverse cutaneous drug reactions. This will include a detailed description of the types of cutaneous drug reactions that appear most commonly, and a discussion of CTCAE grading as it relates to cutaneous drug reactions.

Attendance at this event is pending approval for 1 contact hour of clinical research education on applications for Maintenance of ACRP's CCRC®, CCRA®, CPI® or ACRP-CP® certification designations

Presenter: Aida Lugo-Somolinos, MD, FAAD
Professor, Dermatology
Director, Clinical Trials Unit
UNC School of Medicine

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You can also dial in to the meeting. Call the number 1-929-205-6099 and enter the access code: 996 2695 3748 when prompted

TraCS Tales of Translation features experienced scientists from academia and industry discussing the many twists and turns that are a part of research careers in the life sciences. Participating scientists will be asked to speak informally about their career decisions and pivot points, what translation means to them, and their advice for early stage researchers. This week's researcher is Lisa Crose, PhD.

Crose is currently a Manager of Regulatory Affairs at Regulatory Professionals, Inc. (RPI), a consulting firm that provides regulatory expertise to the pharmaceutical industry. In this role, she supports drug development programs across therapeutic areas by developing feasibility and regulatory strategy, evaluating safety and efficacy data, preparing regulatory documents, and attending meetings on behalf of clients at the US Food and Drug Administration. Before her regulatory career, Lisa earned her Ph.D. in Pharmacology from the University of North Carolina at Chapel Hill and was a Postdoctoral Associate in the Department of Pediatrics at Duke University Medical Center.

There will be a Q&A session at the end.

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