Accountable for strategy and implementation of complex business initiatives within the Project Management Office. Owns organizational project quality risk management.Consults across the organization to streamline and create efficiencies for clinical development. Identifies strategic opportunities and drives continuous improvement.

Accountable for strategic oversight of client clinical research programs in oncology and rare disease spanning from FIH to late phase. Responsible for escalations related to operations and execution of clinical research studies including development and improvements for scope, budgets, timelines, people, SOPs and systems. Provide supervision, growth and development opportunities to direct reports.

Focused on agile biotech clients in early phase oncology research

Strategic development for oncology clinical operations partnerships and trial enrollment optimization. Development and leadership across global clinical operations communications including organizational change management capabilities related to monitoring

Clinical Project Management Consultant managing work for the oncology therapeutic area with a specific clinical focus on Cyramza (ramucirumab). Responsible for global expanded access programs (compassionate use), Phase 3 clinical trials and global regulatory submissions. Based in South Florida as a high performing remote teleworker.

Oncology therapeutic area; investigator site training

Lean Six Sigma, Kaizen, DMAIC/DMEDI, Continuous improvement

Responsible for site submission package for site activation through closeout: preparation/compilation of full ethical review board submission package both at trial and site level including creation of informed consent document

Supported a number of oncology medical directors, operational directors and managers. Led cross-functional administrative team through organizational wide process improvement.

High intensity boot camp; interval training; strength and endurance; spin