Job Title: Global Trial Manager, Late Phase Studies, Single-Sponsor Dedicated (home-based in Europe), Dublin
Client:IQVIA
Location:Dublin, Ireland
Job Category:Other
EU work permit required:Yes
Job Reference:be4028725853
Job Views:11
Posted:30.06.2025
Expiry Date:14.08.2025
Job Description:
Job Purpose: As Senior Global Trial Manager, you will contribute to all aspects of assigned clinical trials to deliver outcomes within schedule, budget, quality, and compliance standards. You will lead specific aspects of global trials and become a core member of the Clinical Trial Team (CTT).
Key Responsibilities:
Study essential documents: Development of protocol sections, study tools, guidelines, training materials, and contributions to regulatory documents.
Project Management: Ensure timely reporting, support drug supply management, implement issue resolution, handle trial close-out activities, and manage trial budget and data review plans.
Vendor Management: Develop outsourcing specifications, manage CRO relationships, and ensure quality standards.
Internal and external collaboration: Organize trial committees, act as site contact, manage interactions with line functions, and report progress at CTT meetings.
Ideal Background:
Advanced degree in life sciences or healthcare preferred.
2-5 years of experience managing late-phase global clinical trials.
Experience with Non-Interventional Studies and regulatory safety documents.
Strong skills in protocol development, communication, organization, and networking.
Knowledge of GCP, clinical trial design, and drug development process.
Passion for late-phase studies.
IQVIA is a leading provider of clinical research services, insights, and healthcare intelligence. We value diversity and inclusion, fostering a culture of belonging and innovation.
Note: Non-passport holders may need a work permit. All applications should be submitted via the 'Apply now' button. Do not provide bank or payment details during application.
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