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Trial Delivery Specialist/ Clinical Trial Coordination, FSP

3 Locations💼 Full-time🗓 2026-01-16 → 2026-07-31

Core

Execution-focused global role driving collaboration across internal and external partners to ensure operational excellence in clinical study management across all phases and therapeutic areas.

Role type

Trial Delivery Specialist / Clinical Trial Coordinator

Builds

Clinical studies for a leading global biopharmaceutical company advancing vaccines, general medicines, and specialty medicines

Domain

Biopharmaceuticals / Clinical Research

Deliverable

client delivery

Required skills

Project management, risk management, vendor management, CRO oversight, study planning, data oversight, budget management, regulatory knowledge

Preferred skills

Clinical trial management systems proficiency, Microsoft Office tools, ability to manage multiple priorities

Responsibilities

Monitor study conduct and progress, resolve and escalate risks; manage end-to-end operational study delivery activities; review key clinical documents and support study plan development; coordinate study-related activities and cross-functional team communication; support country oversight activities including recruitment and compliance tracking; oversee vendor management and CRO deliverables; oversee delivery of clinical supplies and study materials; ensure eTMF data completeness and inspection readiness; manage change orders, expenses, and financial consistency

Seniority

Entry-level to Junior, hands-on IC

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