Senior Global Trial Lead – Late-Phase Studies

IQVIA; Dublin; On-site; EUR 90,000 - 120,000; Full time

Job summary

IQVIA is seeking a Senior Global Trial Manager to lead late‑phase global studies within the Single Sponsor Department. You will own study deliverables, timelines, budgets, and quality, partnering across functions to drive successful outcomes.

Role demands an advanced life sciences degree and 2–5 years of global Phase IV/NIS trial experience, with strong skills in protocol development, regulatory writing, and cross‑functional collaboration.

Qualifications

• Experience managing late‑phase global trials (Phase IV, PASS, PAES, or NIS).
• Proven ability to lead protocol development, study startup, and regulatory writing.
• Strong communication, organizational, and collaboration skills.
• Deep understanding of GCP and clinical trial design.
• Interest in real‑world evidence and patient outcomes.

Responsibilities

• Draft and oversee sections of study documents, data reviews, and regulatory submissions.
• Lead project governance, timelines, budgets, and TMF audit readiness; manage drug supply forecasting.
• Coordinate CRO/vendor selection and cross‑functional collaboration with data management and regulatory teams.

Skills

Global trial management

Protocol development

Regulatory writing

Vendor & stakeholder management

Cross-functional collaboration

GCP knowledge

Education

Advanced degree in life sciences or healthcare

Job description

IQVIA is seeking a Senior Global Trial Manager to lead late‑phase global studies within the Single Sponsor Department. You will own study deliverables, timelines, budgets, and quality, partnering across functions to drive successful outcomes.

Role demands an advanced life sciences degree and 2–5 years of global Phase IV/NIS trial experience, with strong skills in protocol development, regulatory writing, and cross‑functional collaboration.