Experteer Overview

Por favor, asegúrese de leer completamente el resumen y los requisitos de esta oportunidad de empleo que se detallan a continuación.

In this role you will lead clinical trial management across programmes, ensuring timelines, budgets, and quality standards are met. You will work with cross-functional teams to implement protocols, build strong investigator relationships, and ensure regulatory and ethical compliance. You will solve design, vendor, and risk issues to deliver high-quality trial outcomes.

This position offers home-based work in Spain or the UK and the chance to contribute to ICON’s mission of advancing clinical development.

Compensaciones / Beneficios

- Plan and manage all aspects of clinical trials, ensuring timelines, budget, and quality standards
- Collaborate with cross-functional teams to implement clinical trial protocols and procedures
- Build and manage relationships with trial investigators and stakeholders




- Ensure trials comply with local, national, and international regulations and ethical guidelines
- Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management

Responsabilidades

- University degree in medicine, science, or equivalent combination of education u0026 experience
- Demonstrated ability to drive the clinical deliverables of a xugodme study
- Subject matter expertise in the designated therapeutic area
- Prior monitoring experience is preferred
- Willingness to travel approximately 25%

Requisitos principales

- Annual leave entitlements
- Health insurance offerings
- Competitive retirement planning
- General Employee Assistance Programme (LifeWorks)
- Life assurance
- Flexible country-specific optional benefits

📌 Clinical Trial Manager (Madrid)
🏢 Icon Clinical
📍 Madrid