Global Study Manager: Lead Cross-Functional Clinical Trials

IQVIA; Madrid; On-site; EUR 39,000 - 93,000; Full time

Job summary

IQVIA in Madrid seeks a Global Study Manager to join the Clinical Operations team, supporting delivery of global studies from protocol development to CSR and archiving.

The role collaborates with internal and external partners, manages study documents, budgets, timelines, and quality controls, ensuring inspection readiness and adherence to ICH/GCP guidelines across outsourced and in-house activities. Fluent English required.

Qualifications

• University degree in medical or biological sciences.
• Experience in pharma/clinical research is preferred.
• Strong knowledge of ICH/GCP.

Responsibilities

• Leads preparation of delegated study documents.
• Manages interactions with CROs and external providers.
• Plans and conducts study meetings with investigators/monitors.
• Ensures supply of Investigational Product and materials.
• Supports budget management and invoice reconciliation.
• Ensures quality and trial master file readiness.

Skills

Communication

Project management

Leadership

Independence

English proficiency

Education

Bachelor's degree in medical or biological sciences

Tools

MS Office

Job description

IQVIA in Madrid seeks a Global Study Manager to join the Clinical Operations team, supporting delivery of global studies from protocol development to CSR and archiving.

The role collaborates with internal and external partners, manages study documents, budgets, timelines, and quality controls, ensuring inspection readiness and adherence to ICH/GCP guidelines across outsourced and in-house activities. Fluent English required.