Remote Senior Clinical Data Lead

IQVIA Holdings Inc.; United States; Remoto; USD 140.000 - 190.000; Tempo pieno

Descrizione del lavoro

IQVIA is hiring multiple Clinical Data Management Leads to oversee end-to-end data management for global clinical trials in a fully remote/WFH setup. You will serve as the client contact for deliverables and manage timelines, budgets, and resources while mentoring teams and ensuring regulatory compliance.

Qualified candidates bring 10+ years in CDM, 5+ years in a Lead CDM role, and expertise in Medidata Rave or Oracle InForm within global studies of 1000+ patients.

Competenze

• Bachelor's degree in life sciences, health, clinical, biological, or mathematical field.
• 10+ years of direct clinical data management experience with 5+ years in a Lead CDM role.
• Experience leading complex global studies (1000+ patients).
• Expertise with Medidata Rave, Oracle InForm, or similar EDC systems.
• Strong knowledge of GCP, ICH, and regulatory processes.
• Excellent communication and leadership skills.

Mansioni

• Lead data management for global clinical trials from study setup to database lock.
• Serve as the main client contact for all 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.

Conoscenze

Leadership

Data management

Client communication

Regulatory compliance

Project management

Formazione

Bachelor's degree in life sciences/health/clinical/biological/mathematical field

Strumenti

Medidata Rave

Oracle InForm

Descrizione del lavoro

IQVIA is hiring multiple Clinical Data Management Leads to oversee end-to-end data management for global clinical trials in a fully remote/WFH setup. You will serve as the client contact for deliverables and manage timelines, budgets, and resources while mentoring teams and ensuring regulatory compliance.

Qualified candidates bring 10+ years in CDM, 5+ years in a Lead CDM role, and expertise in Medidata Rave or Oracle InForm within global studies of 1000+ patients.