If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person. Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week . Our head office is purposely designed with collaboration in mind, providing space where teams can come together to strategize, brainstorm and connect on key projects.

Our dedication to sustainability is also central to our culture and part of what makes AstraZeneca a great place to work. We know the health of people, the planet and our business are interconnected which is why we're taking ambitious action to tackle some of the biggest challenges of our time, from climate change to access to healthcare and disease prevention. As a Clinical Data Manager I, you will support the delivery of high-quality clinical data for assigned studies and indications across different Data Management sourcing models.

Working under the guidance of an experienced Data Management Lead, you will contribute to a variety of data management activities while ensuring data quality and operational excellence. You will collaborate with general study teams and external partners, including CRAs and data providers,



to support day-to-day clinical data management activities. This role offers an excellent opportunity to develop your expertise and contribute to the successful execution of clinical studies in a global environment. documentation review and/or creation, User Access Testing, query management, data cleaning and reviews, third party data reconciliation in accordance with the project study model, KPIs and timelines.). provide data toclinicalteams forperformingmedicalandclinicalreviews,coordinationofinstreamdatareview, labdatareview,etc.); - snapshots, interim, and migrations); - SupportDMDeliveryLeadstomaintainCDMspecifiedsystemsandtypesofdeliverables,milestoneachievements, risks and mitigations and data transfer agreements, and other study administrative needs.

Mayincludeactivities related to study expected document Lists and quality compliance checks. Attentiontodetailtoensure quality.

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Media, Follow AstraZeneca on LinkedIn Follow AstraZeneca on Facebook Powering Scientific Innovation - YouTube Such accommodation is available on request in respect of all aspects of the recruitment, assessment and selection process and may be requested by emailing [emailprotected]. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.

📌 Clinical Programmer I (Galicia)
🏢 AstraZeneca
📍 Galicia