Experteer OverviewIn this role you support high-quality clinical data delivery for assigned studies within a general environment. You work under a Data Management Lead to perform essential CDM activities, ensuring data quality and timely deliverables. You collaborate with study teams, external partners, and vendors to support start-up, conduct, and closeout phases, while helping maintain audit readiness and process improvements. This is an opportunity to grow in clinical data management within a mission-driven, collaborative culture focused on patients and sustainable pensaciones / Beneficios
- Provide study-level CDM administrative support across study start-up, conduct, and closeout phases
- Review and create documentation, perform User Access Testing, manage queries, and support data cleaning and third-party data reconciliation
- Generate study status reports and coordinate data reviews with clinical teams
- Coordinate with Data Management Vendor on deliverables, milestones, snapshots, migrations




- Oversee data quality and documentation quality of deliverables and milestones
- Support DM Delivery Leads to maintain CDM systems, deliverables, risks, mitigations, and data transfer agreements
- Assist with Trial Master File compliance and quality checks
- Support User Acceptance Testing of (internal/external) electronic Data Capture systems
- Contribute to issue resolution and continuous improvement in CDM processes
- Handle ad-hoc CDM requests as needed by DM LeadsResponsabilidades
- University or college degree in life sciences or related subject, pharmacy, nursing or equivalent
- Fluent English (oral and written)
- Attention to detail and quality mindset
- Strong verbal and written communication skills
- Ability to manage multiple projects simultaneously and meet deadlines
- Good interpersonal skills and experience communicating in a global environment

📌 Clinical Programmer I (Barcelona)
🏢 AstraZeneca
📍 Barcelona