Senior Clinical Data Manager II role based in Barcelona (3 days on-site weekly) leading clinical data management across integral studies. Responsibilities include coordinating CDM deliverables, overseeing vendor partnerships, ensuring data quality and regulatory compliance, and mentoring junior colleagues.
Responsibilities
- Coordinate clinical data management deliverables for assigned studies as primary study contact
- Act as lead point of contact for data management vendors; oversee team performance and budgets
- Identify, mitigate and escalate operational risks affecting study delivery and timelines
- Drive adherence to corporate and therapeutic data standards; ensure database integrity and analysis readiness
- Support regulatory inspection readiness and Trial Master File compliance activities





Requirements
- University degree in life sciences, pharmacy, nursing, or equivalent field
- Clinical Data Management experience in Biotech, Pharma, or CRO industry
- Knowledge of Good Clinical Data Management Practices and relevant regulatory requirements
- Experience with clinical databases, EDC systems, and data management platforms
- Demonstrated expertise in query management and data reconciliation processes
- Fluency in English; excellent written and verbal communication skills
- Ability to manage multiple concurrent projects with strong organizational skills

📌 Senior Clinical Data Manager II (España)
🏢 AstraZeneca
📍 España