Cathy Radovich

cradovic@med.umich.edu 734.998.6059
Cathy Radovich Cathy Radovich has held previous positions at the director and management level, including director of clinical development at QuatRx Pharmaceuticals, manager of clinical trial design and application engineering at PhaseForward, and several positions of increasing responsibility for Warner Lambert/Parke Davis – Pfizer. As an independent consultant for Clinical Trials and Technology, she managed clinical and data teams in support of clinical trial research leading to NDA submission. She has served as an advisory board member to leading electronic data capture and clinical research organizations. She has published her work on Remote Source Data Verification (rSDV) in support of “cleaner data faster.” She has more than 15 years of experience in the health care and pharmaceutical industries, with expertise in data management, electronic data capture, and clinical trial management in development Phases I–III.

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