Global Trial Manager, Late Phase Studies, Single-Sponsor Dedicated (home-based in Europe) Join to apply for the Global Trial Manager, Late Phase Studies, Single-Sponsor Dedicated (home-based in Europe) role at IQVIA .
Position Overview We are seeking a Senior Global Trial Manager to join our Single Sponsor Department, dedicated exclusively to Novartis .
In this role, you will manage late-phase clinical trials at a global level, ensuring they meet timelines, budgets, and quality standards.
As a key member of the Clinical Trial Team (CTT), you will lead critical aspects of global studies and collaborate across functions to drive success.
Responsibilities Draft protocols, CRFs, training materials, and data review plans.
Contribute to safety updates, IBs, and regulatory submissions.
Oversee data review and TMF audit readiness.
Forecast and manage investigational product supply.
Support study closeout, issue resolution, and lifecycle budget tracking.
Coordinate CRO/vendor selection and performance.
Facilitate advisory boards and serve as site liaison.
Lead cross-functional collaboration with data management, drug supply, and others.
Qualifications Advanced degree in life sciences or healthcare.
2–5 years' global experience managing phase IV, PASS, PAES, or NIS trials.
Strong record in protocol development, study startup, and regulatory writing.
Excellent communication, organizational, and collaboration skills.
Deep understanding of GCP and clinical trial design.
Passion for advancing real-world evidence and patient outcomes.
This role is not eligible for UK VISA sponsorship.
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