Descrizione del lavoro:
Global Trial Manager
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
We are currently seeking an Oncology Global Study Manager to join our diverse and dynamic team. In this role, you will lead and coordinate global study activities, ensuring delivery on time, within budget, and to the highest quality standards. You will oversee all aspects of study execution, from planning and resource management to stakeholder communication and risk mitigation.
Aligned to a global biopharmaceutical company, you can expect to be involved in end-to-end study operational oversight, cross-functional leadership and vendor coordination, and quality, compliance, and inspection-readiness activities.
Please see below for additional responsibilities:
Role Responsibilities
* Developing and managing detailed study plans, including timelines, budgets, and resource allocation, to ensure successful delivery.
* Leading cross-functional study teams, coordinating activities to meet study objectives, and facilitating effective communication and collaboration.
* Monitoring study progress, identifying risks and issues, and implementing mitigation strategies to keep the study on track.
* Engaging with stakeholders to manage expectations, provide updates, and ensure alignment with study goals and organisational priorities.
* Preparing and presenting study reports, status updates, and performance metrics to senior management and other key stakeholders.
Your Profile
* Bachelor's degree in project management or a scientific discipline is preferred, along with significant experience in clinical project management and team leadership.
* Proven track record of managing Oncology global clinical trials from initiation to close-out, with strong delivery across scope, timelines, and budget.
* Strong leadership and organisational skills, with the ability to manage cross-functional teams and prioritise effectively.
* Excellent communication and interpersonal skills, with the ability to build strong relationships and manage stakeholder expectations.
* Proficiency with project management tools and methodologies; certifications such as PMP or PRINCE2 are advantageous.
* Detail-oriented, proactive, and adaptable, with a commitment to achieving study goals and driving continuous improvement.
This home-based role can be based in a number of European countries.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
* Competitive base salary and performance related incentives
* Health and wellbeing programmes including medical, dental, and vision coverage where applicable
* Retirement and pension plans
* Life assurance and disability coverage
* Employee assistance programmes and wellbeing resources
* Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply
| Provenienza: | Web dell'azienda |
| Pubblicato il: | 02 Gui 2026 |
| Tipo di impiego: | Lavoro |
| Settore: | Salute |
| Lingue: | Inglese |
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