Introduction to role: This role is based in Barcelona , with an on-site commitment of three days a week. Fluency in English is required. Are you ready to lead global clinical studies that turn scientific breakthroughs into evidence for life-changing medicines? As a Integral Study Associate Director , you will lead a cross-functional study team from handover through close-out and archiving, serving as the critical link between the study team and the Clinical Program Team. You will own study delivery against agreed timelines, budgets and quality standards, ensuring strong partnerships across internal functions and external partners so patients can benefit sooner. You will set the direction, remove obstacles and uphold inspection readiness, while amplifying the impact of every function involved in the study.



Your leadership will translate complex plans into predictable execution—shaping data that informs program decisions, regulatory submissions and patient access. Can you see yourself orchestrating multi-country operations with clarity, pace and quality?

Accountabilities:

- Lead, provide guidance and delegate appropriately to a cross-functional study team or oversee outsourced delivery activities to ensure the clinical study progresses as planned, driving achievement of milestones according to timelines, budget and quality standards. May hold accountability and]]>

📌 Global Study Associate Director (Barcelona)
🏢 AstraZeneca
📍 Barcelona