Global Trial Manager, Late Phase Studies, Single-Sponsor Dedicated (home-based in Poland)

IQVIA Holdings Inc.

Job Overview

Location

Warsaw, Poland

Job Type

Full-time

Full Job Description

📋 Description

• We are looking for a Senior Global Trial Manager to join our Single Sponsor Department.
• As a core Clinical Trial Team (CTT) member, you’ll lead critical aspects of global studies and collaborate across functions to drive success.
• You’ll have the opportunity to specialise in one for 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

🎯 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

🏖️ Benefits

• The potential base pay range for this role, when annualized, is 171 500,00 zł - 404 600,00 zł
• Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits

Skills & Technologies

GCP

Onsite

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IQVIA Holdings Inc.

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About IQVIA Holdings Inc.

IQVIA Holdings Inc. provides advanced analytics, technology solutions, and clinical research services to the life-sciences industry. Formed through the 2016 merger of Quintiles and IMS Health, the company integrates healthcare data, analytics, and domain expertise to help biopharmaceutical and medical-device clients optimize drug development, commercialization, and real-world evidence generation. Its offerings span clinical trial design and execution, real-world insights, commercial strategy, and technology platforms that connect stakeholders across the healthcare ecosystem. Headquartered in Durham, North Carolina, IQVIA operates in more than 100 countries, supporting the development and delivery of therapies to improve patient outcomes worldwide.

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