CanadaLead Cisco service adoption, renewals, and expansion for CDW customers in partnership with sales, presales, and delivery teams. Serve as a strategic advisor throughout the customer lifecycle, from implementation through optimization.
Join EveryMatrix as a Business Analyst shaping iGaming configuration requirements, workflows, integrations, and automation. The role supports AI-enabled process improvements across business, product, development, and operations teams.
Monitor oncology clinical trials across Poland for a global research organization. Support site compliance, data quality, essential documentation, and inspection readiness through remote and on-site activities.
Senior Clinical Research Associate overseeing gastrointestinal clinical trial monitoring across Serbia and Croatia. The role supports site compliance, recruitment, study documentation, and CRA mentoring at Alimentiv, a global CRO.
Supports cross-functional clinical research studies by coordinating vendors, sites, data, budgets, timelines, and regulatory compliance.
United States
New YorkLead clinical science activities for gynecologic oncology programs at Syneos Health, supporting medical data review, safety assessment, and eligibility decisions. Coordinate study teams, project deliverables, expert input, and medical review processes across integrated drug development projects.
United States
Kentucky
OhioSupport AbbVie’s oncology clinical trials through site monitoring, investigator collaboration, and risk management. Help maintain data integrity, recruitment, compliance, and patient safety across trial activities.
Coordinate sponsor-dedicated clinical trials for ICON across global research programs. Maintain protocol compliance, site oversight, data quality, and timely study execution.
Lead clinical research activities for Danaher Diagnostics across in vitro diagnostic and medical device trials. Manage study sites, monitor data, and support compliance with FDA requirements and Good Clinical Practice.
Monitor sponsor-dedicated pharmaceutical trials for ICON in a primarily home-based role. Support protocol compliance, data integrity, patient safety, and reliable clinical data throughout each study.
