United StatesSupport regional clinical study delivery, trial documentation, study systems, and budgets at BeOne Medicines. The company develops cancer medicines and therapies.
Support ICON’s sponsor-dedicated clinical trials from Mexico by coordinating study records, regulatory submissions, trial materials, and milestone tracking.
United StatesSupport Linical’s clinical research programs through trial documentation, TMF administration, regulatory submissions, site support, and coordination with study teams.
Support documentation, compliance, coordination, and performance tracking for sponsor-dedicated clinical trials at ICON in Mexico.
Support the coordination, documentation, and reporting of clinical trials for ICON’s sponsor-dedicated pharmaceutical programs. This hybrid full-time role is based in Mechelen, Belgium, with a mix of office and home working.
United States
MassachusettsSupport clinical operations for PathAI’s AI-powered pathology trials as a Clinical Trial Associate. Coordinate laboratory services, investigator sites, specimens, and Clinical Trial Manager deliverables.
Support clinical trial administration and operational delivery for ICON’s sponsor-dedicated pharmaceutical services. Coordinate regulatory documentation, site communications, trial records, and stakeholder activities.
Poland
Romania
SerbiaSupport global clinical study teams at Parexel across trial operations, documentation, submissions, supplies, meetings, and Trial Master File maintenance. Coordinate study information and communications across affiliates, vendors, and internal stakeholders.
