Senior Clinical Data Manager – Global Trials (Remote)

IQVIA Inc; Dublin; A distancia; EUR 110.000 - 150.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Fully remote role

Equipment provided

Competitive salary

Career growth

Global culture

Descripción de la vacante

IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management for global clinical trials. This fully remote role provides company equipment and focuses on quality, compliance, and cross-functional leadership.

Ideal candidates have 10+ years in CDM, with 5+ years in a lead role, and strong expertise in Medidata Rave and Oracle InForm to drive regulatory-compliant data delivery.

Formación

• Bachelor’s degree in life sciences, health, clinical, biological, or mathematical field.
• 10+ years of direct clinical data management experience, 5+ years in a Lead CDM role.
• Roles may include Clinical Data Manager, Senior CDM, Lead Data Manager, Principal Data Manager, or Data Management PM.
• Experience with large global studies (1000+ patients).
• Expertise with Medidata Rave, Oracle InForm, or similar EDC systems.
• Strong understanding of GCP, ICH, and clinical research processes.
• Excellent communication and leadership skills.

Responsabilidades

• Lead data management for complex, global clinical trials from study setup to database lock.
• Serve as main client contact for data management deliverables.
• Oversee SAE, PK, and external data reconciliation and database deployment.
• Manage timelines, budgets, and resource allocation to meet customer expectations.
• Mentor junior data management staff and promote best practices.
• Drive process improvements and ensure regulatory and SOP compliance.

Conocimientos

Leadership

Communication

GCP/ICH knowledge

Project management

Educación

Bachelor’s degree in life sciences/health/clinical/biological/mathematical

Herramientas

Medidata Rave

Oracle InForm

Descripción del empleo

IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management for global clinical trials. This fully remote role provides company equipment and focuses on quality, compliance, and cross-functional leadership.

Ideal candidates have 10+ years in CDM, with 5+ years in a lead role, and strong expertise in Medidata Rave and Oracle InForm to drive regulatory-compliant data delivery.