Clinical Operations Expert
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Dynamic and results-driven Project Manager in Clinical Study Start-up and site maintenance, with over 15 years of experience in significantly enhancing site productivity and leading teams. This most recent experience includes feasibility studies, site identification, regulatory reviews, and site maintenance. I excel at aligning cross-functional objectives and implementing best practices.
With a proven ability to interpret and create strategic proposals for clinical operations, I develop comprehensive global resource plans and accurately oversee time-reporting activities.
Clinical trial phase experience includes Screening, Phase I, II, and III, as well as real-world evidence studies. Therapeutic expertise encompasses oncology, molecular biology, blood-based assays, solid tumors, hematology, and nephrology, with a focus on monitoring experience in Type I and Type II Diabetes Mellitus (Phases II and III).
Bachelor of Arts degree in Audiology and Speech Pathology, 1990, The University of Tennessee, Knoxville, TN
