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.annual leave entitlementshealth insurance offeringsEmployee Assistance Programme (EAP)life assuranceflexible country-specific benefitsPlan, setup, and execute global clinical studies across regionsOversee country teams and third-party vendors for smooth deliveryCollaborate with AstraZeneca internal teams and external partnersDevelop 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 standardsSupport risk management, QA activities, audits, and inspectionsMaintain inspection readiness and comprehensive study documentationBachelor’s degree in life sciences or related field5+ years in clinical research with 3+ years in integral project management/GSM in Pharma or CROStrong knowledge of ICH-GCP regulationsProven track record delivering studies on time, on budget, to qualityExperience with internal and external vendor management and budgetingExcellent communication, teamwork, and problem-solving skillsAbility to manage multiple priorities in a matrix environmentExperience across all phases of clinical study lifecycleExperience in haematology or oncology early-phase studiesExperience using AI automation in daily work as a GSMKnowledge of GXP beyond GCP (e.g., GMP, GLP)teamworkproblem-solvingICH-GCP knowledgeclinical study lifecycle

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