Global Study Lead — Cross-Functional Delivery

IQVIA Argentina; Madrid; Presencial; EUR 52.000 - 97.000; Jornada completa

Descripción de la vacante

IQVIA in Madrid seeks a Global Study Associate Director (GSAD) to lead cross-functional study teams and drive delivery of clinical trials on time, within budget and to high quality standards. You will be the main liaison from study handover through to close-out, coordinating with external partners and the Clinical Program Team.

The role requires extensive ICH-GCP knowledge, SOP adherence and strong leadership, communication and strategic thinking to manage risk, quality, TMF and inspections,

Formación

• University degree in medical or biological sciences or related field.
• 5 years of relevant clinical experience in the pharmaceutical industry including 2 years of project management.
• Knowledge of ICH-GCP and regulatory requirements; strong leadership and collaboration skills.

Responsabilidades

• Lead cross-functional study teams or oversee outsourced delivery to meet milestones, timelines, budget and quality.
• Coordinate investigator meetings and study-related communications across functions and external partners.
• Develop and maintain essential study documents and oversee TMF; ensure compliance with SOPs and regulations.
• Monitor study plans, KPIs, risk management, and escalate issues with mitigations to CPT and sDSM/DSM.
• Ensure audit readiness and provide feedback for team development and process improvements.

Conocimientos

Team leadership

Project management

Communication

Strategic thinking

Prioritization

Conflict management

Educación

Bachelor's degree

Clinical research knowledge

Descripción del empleo

IQVIA in Madrid seeks a Global Study Associate Director (GSAD) to lead cross-functional study teams and drive delivery of clinical trials on time, within budget and to high quality standards. You will be the main liaison from study handover through to close-out, coordinating with external partners and the Clinical Program Team.

The role requires extensive ICH-GCP knowledge, SOP adherence and strong leadership, communication and strategic thinking to manage risk, quality, TMF and inspections,