Global Study Associate Manager — Barcelona

Alexion Pharma Spain S.L.; Barcelona; On-site; EUR 65,000 - 90,000; Full time

Job summary

Alexion Pharma Spain S.L. in Barcelona seeks a Global Study Associate Manager to support clinical study execution from CSP development through CSR and archiving.

You will collaborate with the global study team, manage vendor oversight, and ensure timelines and quality in studies across multiple therapeutic areas. The role emphasizes document preparation, cross-functional coordination with Data Management, Regulatory, and Quality Assurance, plus budget support and risk mitigation.

Qualifications

• Bachelor's degree in life sciences, health care, or drug development or equivalent work experience.
• Proficiency with Microsoft Office (Excel, PowerPoint, SharePoint Online), eTMF, and Veeva Systems.
• Excellent organizational, communication, and time management skills.
• Highly proactive and willing to take initiative.
• Strong relationship-building skills.

Responsibilities

• Support activities for clinical study execution, ensuring adherence to timelines and quality standards.
• Lead document preparation for studies and vendor-related documents (Vendor Oversight Plan).
• Maintain interactions with cross-functional teams (Data Management, Procurement, Regulatory, Patient Safety, QA).
• Collaborate with internal and external partners to execute delegated study tasks.
• Contribute to planning and execution of meetings, identify risks and mitigation plans.
• Provide support for project and budget management and SME initiatives.

Skills

Microsoft Office

eTMF

Veeva Systems

Organizational skills

Communication skills

Time management

Relationship building

Education

Bachelor's degree in life sciences or related field

Tools

Microsoft Office

eTMF

Veeva Systems

Job description

Alexion Pharma Spain S.L. in Barcelona seeks a Global Study Associate Manager to support clinical study execution from CSP development through CSR and archiving.

You will collaborate with the global study team, manage vendor oversight, and ensure timelines and quality in studies across multiple therapeutic areas. The role emphasizes document preparation, cross-functional coordination with Data Management, Regulatory, and Quality Assurance, plus budget support and risk mitigation.