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Global trial manager, late phase studies, single-sponsor dedicated (home-based in europe)

Dublin
IQVIA
Trial manager
Posted: 12h ago
Offer description

Senior Global Trial Manager – Single Sponsor
Are you experienced in managing late phase clinical trials at a global level?
We are looking for a Senior Global Trial Manager to join our Single Sponsor Department.
Join our global team and take ownership of delivering late‑phase clinical trials that meet timelines, budgets, and quality standards. As a core Clinical Trial Team (CTT) member, you'll lead critical aspects of global studies and collaborate across functions to drive success.
As part of your role, you’ll have the opportunity to specialise in one of the following areas:

Scientific Review Committee (SRC)
Non‑Interventional Studies (NIS)
Managed Access Programs (MAP)
Investigator‑Initiated Trials (IITs)
Research Collaborations (RCs)
Program Level Documents (PLD)

Key Responsibilities
Clinical Documentation & Study Tools

Draft sections of protocols, CRFs, training materials, and data review plans
Contribute to the development of safety updates, IBs, and regulatory submissions

Project Leadership

Oversee data review and TMF audit readiness
Forecast/manage investigational product supply
Support study closeout, issue resolution, and lifecycle budget tracking
Contribute to Managed Access Program coordination and compliance

Vendor & Stakeholder Management

Coordinate CRO/vendor selection and performance
Facilitate advisory boards (DMCs/Steering Committees) and serve as the site liaison
Lead cross‑functional collaboration with data management, drug supply, and more

What You’ll Bring

Advanced degree in life sciences or healthcare
2–5 years' global experience managing phase IV, PASS, PAES, or NIS trials
Strong track record in protocol development, study startup, and regulatory writing (e.g. PSURs, DSURs, NDA/BLA reports)
Excellent communication, organizational, and collaboration skills
Deep understanding of GCP and clinical trial design
Passion for advancing real‑world evidence and patient outcomes

Please note this role is not eligible for the UK visa sponsorship.
Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered.
EEO Minorities/Females/Protected Veterans/Disabled
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