Executive Bio:
17 years of Clinical Operations, Medical affairs, Clinical Trials Site Research, Management expertise in Clinical Research, Managed Care, Health Outcomes in:
•Business Development, partnership agreements for technology based solutions to support clinical trials, IRB, EDC/CTMS/ePRO, IRT, Imaging, Labs, dashboards & document management
•VP Medical Affairs for a eClinical (Clinical Trials) research solutions company
•Constructing articles on, ePRO analysis, pharmacoeconomics and financial management of clinical trial research sites and eClinical software.
•Presentations at Medical Conferences for Clinical Research, Webinars on clinical research technology
•Clinical Development Operations analysis, providing technology solutions for clinical and financial data management, Trial Phases 1, , , 4 including REMS/Post Marketing, Patient Recruitment
•EMR – Clinical research database query research, working with key EMR vendors
•Developed and analyzed data for AMCP style FDA dossier submissions
Clinical practice outcomes, P4P, clinical operations Managed care markets, P4P, benchmarking, quality scorecards
•Consultant Pharmaceutical & biotechnology and related companies
Site focused, KOL development = identification & education of protocol and MOA, enrollment, site initiation visits,
•Database development – EDC/CTMS, ePRO, IVRS/IWRS,