Experteer Overview
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In this role you will lead global oncology trials from protocol to Clinical Study Report, ensuring quality, compliance and timely data delivery. You will work with cross-functional experts to activate sites across multiple geographies and drive data readiness, risk management and sponsor communication. You’ll enable rapid decision-making, balance speed with rigor, and support inspection readiness. This position offers the chance to shape large-scale studies and impact patient outcomes in oncology.
Compensaciones / Ventajas
• Lead study document development, updates, and amendments ensuring template/version compliance
• Direct country start-up activities, confidentiality agreements and submissions for rapid site activation
• Oversee vendor strategy, SOW assessments, budgets, change orders and performance to quality, timeline, cost
• Contribute to data management by providing input to CRF and data validation specs and coordinating with sites
• Initiate contracts and budgets, monitor deliverables and spend against approved budgets




• Coordinate supply and investigational products with internal and external teams to ensure uninterrupted trial conduct
• Oversee recruitment, risk management, and quality oversight to protect timelines and data integrity
• Support insurance processes, approvals tracking and renewals for regulatory coverage
• Monitor study progress, identify and escalate issues affecting quality, time or budget
• Support TMF setup, maintenance, inspection readiness, and archiving
• Prepare clear communications for meetings, newsletters and portals to align stakeholders
• Assist with audits and regulatory inspections and ensure robust responses
• Contribute to xqbhyrx SOP reviews and process improvements to share learnings
Responsabilidades
• Bachelor's degree in a relevant field
• 3-4 years progressive clinical trial experience
• Experience with strategic partners and 3rd party vendors
• Excellent knowledge of ICH-GCP principles
• Team-oriented with strong coordination and prioritization skills
• Proactive, flexible, and able to manage multiple tasks
• Strong verbal and written communication skills
• Good negotiation and collaboration abilities
• Some travel may be required
Requisitos principales
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📌 Global Study Manager Early Oncology (Barcelona)
🏢 AstraZeneca
📍 Barcelona