Global Study Manager (Barcelona)

Global Study Manager (Barcelona)

18 sep
|
Icon Clinical
|
Barcelona

18 sep

Icon Clinical

Barcelona

Overview
Presente su candidatura después de leer los siguientes requisitos de habilidades y cualificaciones para este puesto.
As Global Study Manager, you enable global hematology studies in collaboration with AstraZeneca, ensuring timely delivery, budget discipline, and high quality. You work within ICON’s FSP team to integrate with client operations and external vendors, driving study setup, execution, and close-out. You’ll contribute to risk management, QA, and inspection readiness, shaping study documentation and regulatory compliance. This role offers impact through cross-functional partnerships and a focus on early-phase hematology/oncology studies.
Compensaciones / Beneficios
annual leave entitlements
health insurance offerings
retirement planning
Employee Assistance Programme (EAP)
life assurance
flexible country-specific benefits
Responsabilidades
Plan, setup, and execute global clinical studies across regions
Oversee country teams and third-party vendors for smooth delivery
Collaborate with AstraZeneca internal teams and external partners
Develop and update study documents (protocols, ICFs)
Manage contracts and budgets with vendors (e.g., central labs, IRT)




Ensure regulatory compliance (ICH-GCP, AstraZeneca SOPs) and quality standards
Support risk management, QA activities, audits, and inspections
Maintain inspection readiness and comprehensive study documentation
Requisitos principales
Bachelor’s degree in life sciences or related field
5+ years in clinical research with 3+ years in general project management/GSM in Pharma or CRO
Strong knowledge of ICH-GCP regulations
Proven track record delivering studies on time, on budget, to quality
Experience xqbhyrx with internal and external vendor management and budgeting
Excellent communication, teamwork, and problem-solving skills
Ability to manage multiple priorities in a matrix environment
Experience across all phases of clinical study lifecycle
Experience in haematology or oncology early-phase studies
Experience using AI automation in daily work as a GSM
Knowledge of GXP beyond GCP (e.g., GMP, GLP)
excellent communication
teamwork
problem-solving
vendor management
ICH-GCP knowledge
clinical study lifecycle

📌 Global Study Manager (Barcelona)
🏢 Icon Clinical
📍 Barcelona

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