संयुक्त राज्यSupport 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.
संयुक्त राज्यSupport 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.
संयुक्त राज्य
मैसाचुसेट्सSupport 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.
पोलैंड
रोमानिया
सर्बियाSupport 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.
