Ellie Gonzalez Email & Phone Number

Brooklyn, New York, United States

- Partnered with cross-functional teams to define, prioritize and evaluate the feasibility of strategic initiatives across new product developments, regulatory submissions, and clinical validations- Built and managed relationships with partners including CROs, consultants, clinical sites and EDC platforms; oversaw contract negotiation and partner portfolio management to onboard 16 new partnerships- Coordinated workstreams and communications across Product, UI/UX, Clinical Operations, and Compliance teams to gather requirements and achieve milestone delivery within deadlines, budget and quality parameters - Developed program plans comprising of scope, budgets, timelines, and OKRs to manage critical path dependencies, understand resource requirements, and validate whether deliverables met clinical (remove anything that pigeonholes you/screams healthcare if irrelevant) and business requirements- Implemented KPI dashboards, reports and performance measurement tools to track major metrics at a program level, and captured data-driven insights to influence program strategy and resource allocation- Proactively handled issue resolution across the program lifecycle to eliminate blockers, anticipate and mitigate risks, and make trade-off decisions to balance quality outcomes and regulatory standards with total costs

New York, New York, United States

- Headed daily clinical trial operations for 2 clinical trials with complete oversight of patient experience, budgeting, documentation, and regulatory compliance with IRB/HIPAA standards and NYU policies- Devised program plans including scope documents, schedules, work breakdown structures and budgets to govern the activities of a team of 5, benchmark progress to milestones, and assure end-to-end delivery excellence- Introduced new reporting and performance management tools to track key metrics, and generated insightful reports and data visualization to provide status updates and illustrate major cost, quality and compliance trends- Compiled and monitored adherence to IRB guidelines through the clinical trial process, and was the first point of contact for both participants and program teams to address any deviations from plan- Highlight: Guided the completion of both clinical trials within deadlines and budget while managing teams across competing priorities

Denver, Colorado, United States

- Elicited and compiled past medical histories on human research participants, and recorded blood data for research- Performed statistical analysis to draw conclusions from obtained data

Denver, Colorado, United States

- Established and maintained relationships with patients and research participants to guide them through various phases of research studies, answer questions, and ensure a positive participant experience- Administered information and consent requests, and assisted technicians in gathering MRI data for newborn research participants

Denver, Colorado, United States

Level 2, Wine, Passed With Distinction

Bachelor Of Science - Bs, Biology/Biological Sciences, General

Activities and Societies: Graduate from the Honors ProgramMinors: Chemistry and Psychology Concentration: Cognitive Neuroscience