Global Trial Manager, Late Phase Studies

🕒 July 15

🌐 Spain, United Kingdom, +1 more countries – Remote

🇪🇸 Spain – Remote 🇬🇧 United Kingdom – Remote 🇮🇪 Ireland – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

👔 Manager

👻 Ghost score 30%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

💼 Consulting

🏭 Manufacturing

📣 Marketing

💰 $1G Post-IPO Debt on 2023-05

Consulting • Manufacturing • Marketing

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• Draft sections of protocols, CRFs, training materials, and data review plans • Contribute to the development of 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 • Contribute to Managed Access Program coordination and compliance • 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 other functions • Lead critical aspects of global late-phase clinical studies as a Clinical Trial Team member • Deliver trials meeting timelines, budgets, and quality standards

🎯 Requirements

• 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 • Candidates must be based in Madrid, Spain; Reading, Berkshire, United Kingdom; or Dublin, Ireland • This role is not eligible for UK visa sponsorship