At Accell Clinical Research, I lead Phase I–IV clinical trial delivery from study start-up through database lock and closeout, keeping milestones on track across investigator sites, clinical operations, regulatory affairs, data management, safety, medical teams and vendors.
I manage country-level execution, site feasibility and activation, informed-consent processes, recruitment strategy, monitoring-report review, risk management, budgets and inspection readiness. I also coordinate database-lock and closeout activities across cross-functional study teams.
Previously, I coordinated two Phase I–IV trials and supported activation of eight sites, while maintaining study plans, recruitment dashboards, risk logs and governance reporting. My work reduced overdue deliverables by 10% and unresolved site actions and findings by 20%.
I'm PMP-certified and trained in ICH-GCP, with a structured approach to compliance, stakeholder alignment and proactive resolution of operational challenges.
United States