Global Study Manager

Icon Clinical PLC

Industria de Investigación Farmacéutica

Barcelona, Cataluña - Spanien

Project Manager Sénior / Especialista sénior

Híbrido

Experteer Overview

In this Global Study Manager role, you help deliver global hematology clinical studies in early phases within AstraZeneca’s clinical operations framework. You’ll partner with internal teams and external vendors to ensure on-time, on-budget study delivery and high-quality outcomes. You’ll contribute to study setup, execution, risk management, and inspection readiness in a fast-paced, cross-functional environment. This position offers meaningful impact in shaping early-phase hematology research and patient outcomes.

Compensaciones / Beneficios

Annual leave entitlements
Health insurance offerings
Retirement planning options
LifeWorks (24-hour Employee Assistance Programme)
Life assurance
Flexible country-specific benefits

Responsabilidades

Plan, set up, execute, and close-out global clinical studies
Oversee vendors and country teams to ensure smooth study delivery
Collaborate with AstraZeneca internal teams and external partners
Develop and update study documents (protocols, informed consent forms)
Manage third-party vendors, including contracts and budgets
Ensure compliance with regulations (ICH-GCP), AstraZeneca SOPs, and best practices
Contribute to meetings, audits, and inspections
Support risk management and quality assurance efforts
Maintain accurate study documentation and inspection readiness

Requisitos principales

Bachelor's degree in life sciences or related field
≥5 years in clinical research with ≥3 years in global project management/global study management in pharma or CRO
Strong knowledge of ICH-GCP and regulatory requirements
Track record of delivering projects on time and within budget
Experience with vendor setup, management, and budgets (e.g., central labs, IRT)
Excellent communication, teamwork, and problem-solving skills
Ability to manage multiple priorities in a matrix environment
Experience across all phases of the clinical study lifecycle
Experience in haematology or oncology early-phase studies
Experience using AI automation in daily GSM work
Knowledge of GXP beyond GCP (GMP, GLP)