Job Title: Clinical Programmer I Location: Barcelona
At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. 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.
Introduction To Role
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 global 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 general environment.
Accountabilities
Assist with Study level CDM administrative support based on the relevant model and DM Vendor. This may include but is not limited to activities related to the study start up, conduct and closeout phases. (i.E., 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.).
Day to day responsibilities may include but are not limited to: - Study status reporting to the relevant clinical study team members, (e.G., provide data to clinical teams for performing medical and clinical reviews, coordination of instream data review, lab data review, etc.);
- Collaboration with Data Management Vendor regarding upcoming deliverables and milestone achievements (i.E., snapshots, interim, and migrations);
- Oversight of the dataquality, documentation quality, and types of these deliverables and milestones.
Support DM Delivery Leads to maintain CDM specified systems and types of deliverables, milestone achievements, risks and mitigations and data

📌 Clinical Programmer I (Barcelona)
🏢 AstraZeneca
📍 Barcelona