Results-driven Pharma Specialist, with over 15 years in the industry, successful at building strong professional relationships and completing project initiatives on target. Adept at working in cross-functional environments. Excellent written and oral communication skills.
Member of core team which achieved integration of automated vendor feeds with internal project tracking database
Negotiated over $500,000 in waivers for CRO cancellation penalties
Successfully managed 50% increase in assigned projects
Integration and validation of CTMS, IVRS & EDC feeds into internal database for real time monitoring of sites, business analysis and project tracking
MS Project: Risk-assess, identify, monitor trial-level risks
Study Manager for 38 sites in (2) Phase 3 GI studies (no CRO)
Assist with site selection and management of Phase 1 HIV vaccine studies
Successfully resolve GCP audit findings
Project Manage 100+ Phase I bioequivalence studies annually from test product to CSR
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