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

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.

As a core Clinical Trial Team (CTT) member, you'll lead critical aspects of global studies and collaborate across functions to drive success, delivering late-phase clinical trials that meet timelines, budgets, and quality standards.

This is a unique opportunity to specialize in one or more for the following role pathways:

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

·       Advanced degree in life sciences or healthcare

·       Minimum 5 years’ experience in planning, executing and reporting global clinical trials in a pharmaceutical company or CRO, preferably including at least 2 years managing Real World Evidence (RWE) or global late-phase studies (e.g. PASS, PAES, NIS), or relevant equivalent Medical Affairs experience (dependent on role pathway).

·       Experience working in global, cross-functional matrix teams and building effective relationships with internal and external stakeholders.

·       Ability to manage multiple studies or programs of work in parallel, consistently delivering to time, budget and quality expectations.

·       Strong planning, communication, influencing, problem-solving and organisational skills, with the ability to work independently and manage ambiguity and change.

·       A quality and compliance mindset, high attention to detail and the confidence to speak up, challenge constructively and drive issues to resolution.

·       Experience contributing to relevant clinical study documents (e.g. protocols, PSURs, DSURs, regulatory submissions)

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 https://jobs.iqvia.com

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.