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

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 youll lead critical aspects of global studies and collaborate across functions to drive success.

As part of your role youll 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 Youll Bring

Advanced degree in life sciences or healthcare

25 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.

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later in accordance with applicable law. We appreciate your honesty and professionalism.