A trained medical doctor, Dr.FilippouFrye has dedicated her career to the field of clinical trials management working with Stanford's Department of Psychiatry and Behavioral Sciences bridging the important relationships between drug trials sponsors, academic institutions and drug manufacturers. Receiving her Masters of Biosciences from the Keck Graduate Institute, Dr.FilippouFrye has accumulated significant hands-on experience as a project manager evaluating drug trials roll-out effectiveness and customer experience tracking. In addition, Dr.FilippouFrye has organized and taught various hands-on interactive workshops at Stanford University and UC Santa Cruz Silicon Valley Extension Program.
Current Role at Stanford
Create standard operating procedures for the lab and educate research staff on established policies, processes, and procedures.
Supervise the implementation of and adherence to study protocols.
Monitor staffing levels, and identify adequate coverage for trial workload across teams of study coordinators.
Determine effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials.
Audit operations, including laboratory procedures, to ensure compliance with applicable regulations; provide leadership in identifying and implementing corrective actions/processes.
Oversee financial resources, as needed, create internal and external budgets for research protocols, assure financial accountability, and serve as primary liaison between sponsor, department accounting, and Research Management Group.
Assist with analysis of data and preparation of manuscripts and scientific presentations.
Development and implementation of internal mentorship program “Building Success”.
Education & Certifications
MBS, Keck Graduate Institute, Bioscience (2014)
MD, University of Crete, Greece, Medicine (2009)