Global Study Manager
AstraZeneca · Barcelona, Spain
Clinical OperationsFull-timeCompany career page
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Role summary
Global Study Manager supporting clinical trial delivery within AstraZeneca's BioPharmaceuticals Clinical Operations. The role oversees study execution from protocol development through archiving, working cross-functionally with internal teams and external service providers to meet regulatory, quality, and timeline requirements.
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 multiple therapy areas and trial phases
- Expertise in ICH/GCP international guidelines and regulatory compliance
- Advanced project management and external service provider management skills
- Strong verbal and written English communication abilities
- Demonstrated leadership and independent collaboration capabilities
What you'll be doing
- Oversee delegated study document preparation including informed consent forms and clinical study agreements
- Maintain and facilitate cross-functional interactions with internal teams, CROs, and external service providers
- Identify risks and issues, developing mitigation and action plans throughout study lifecycle
- Verify trial master file completeness and quality compliance across assigned study documents
- Support budget management and invoice reconciliation for external service providers
Privacy & handoff
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