Experteer Overview

Consulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo.

In this role you will oversee global study delivery from CSP development through study close-out, coordinating with internal teams and external vendors to ensure on-time, on-budget, and high-quality (CSR-related) deliverables. You will align with the Study Lead and drive vendor scope, oversight, and performance metrics across multiple therapeutic areas. You will manage start-up, recruitment, and site activities, contribute to study documents, and support continuous improvement through lessons learned.

This position offers the opportunity to shape general study execution within a collaborative Development Operations environment.

Compensaciones / Beneficios

- Strategize and oversee key vendors to meet timelines, budget, and quality; maintain oversight documentation across the study life cycle
- Coordinate cross-functional activities including Data Management, Regulatory, Patient Safety, QA, and CROs to enable efficient study delivery
- Plan and conduct internal/external meetings (e.g., Investigators'/Monitors' meetings)
- Support budget management and external service provider invoicing; assist with study documents/plans




- Perform Study Lead activities for less-complex studies and delegate team responsibilities
- Lead lessons learned exercises and contribute to departmental initiatives and SME functions
- Coordinate start-up and recruitment activities across countries and monitor sites globally
- Oversee country activities during protocol amendments, database locks, and Investigator Meetings; manage site close-out and post-trial activities
- Provide study-related training and support country teams with resourcing and CRA development
- Develop/review study documents including training materials and monitoring/oversight plans
- Aggregate and communicate deliverables to the CTT and country xugodme teams
- Support other study and functional activities as assigned

Responsabilidades

- u0026gt;5 years of clinical research experience
- 3 years in a leading role accountable for global trials
- Bachelor's degree or equivalent in clinical practice/health care, life sciences, or drug development
- Excellent organizational, communication, and time management skills
- Highly proactive with initiative and strong relationship-building abilities
- Office-based role requiring computer use, remote communication, problem solving, and cross-team collaboration

Requisitos principales

•

📌 Global Study Manager (Barcelona)
🏢 Alexion Pharmaceuticals
📍 Barcelona