David Beiser

Clinical research can be challenging in the emergency setting. Enrollments are unpredictable, patients are critically-ill, and intervention windows are short. Informed consent in this context can also be challenging, sometimes requires the use of Exception from Informed Consent (EFIC) mechanisms, and requires deep engagement with the community prior to enrolling the first patient.

Education

• Bachelor of Science (B.S.) Cornell University
• Master of Science (M.S.) Northwestern University
• Doctor of Medicine (M.D.) Northwestern University - The Feinberg School of Medicine

Companies

• Director Emergency Trials Unit, University of Chicago (2020)
• Scholar Center for Healthcare Delivery Science and Innovation, University of Chicago (2019)
• Associate Professor University of Chicago (2003)
• Co-founder Qualia Health (2013 — 2020)
• Innovation Fellow, D4Lab Polsky Center for Entrepreneurship, University of Chicago Booth School of Business (2012 — 2013)
• Fellow Argonne National Laboratory (2003 — 2005)
• Medical Product Development Engineer Smith & Nephew Endoscopy (formerly Dyonics) (1990 — 1992)
• Design Engineer, The Design Group Massachusetts General Hospital (1988 — 1990)

Skills

• Emergency Medicine
• Clinical Trials
• Data Analysis

Other

Product Development, Biomedical Engineering, Hospitals, Medical Education, Medical Devices, Clinical Research, Entrepreneurship, Medicine, Healthcare