Global Study Manager - Late Development Oncology
AstraZeneca · Barcelona, Spain
Clinical OperationsFull-timeCompany career page
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Role summary
AstraZeneca seeks a Global Study Manager to oversee late-stage oncology trial execution across multiple countries. The role involves coordinating study delivery, managing external partners and CROs, ensuring regulatory compliance, and maintaining inspection-ready documentation throughout the study lifecycle.
What they're looking for
- University degree in medical, biological sciences, or clinical research-related discipline
- Minimum 3 years pharmaceutical industry or equivalent organizational experience
- Knowledge of clinical development processes across therapy areas and development phases
- Expert-level understanding of ICH/GCP international guidelines
- Strong project management skills with demonstrated ability to lead and collaborate independently
- Advanced computer proficiency and fluent English communication (written and verbal)
- External service provider and vendor management experience
What you'll be doing
- Oversee delegated study execution activities from protocol development through close-out to meet timeline, budget and quality targets
- Coordinate across internal functions and external providers including CROs to ensure consistent delivery across countries
- Lead preparation of study documents and external provider materials ensuring compliance and clarity
- Proactively identify, assess and resolve risks and issues to maintain study momentum and regulatory standing
- Support budget management, invoice reconciliation and CRO oversight with documented quality assurance
Key requirements
- Therapeutic area
- Oncology
Privacy & handoff
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