Senior Global Trial Manager

IQVIA Argentina; Jerez de la Frontera; Presencial; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A leading company in clinical research seeks a Senior Global Trial Manager to lead clinical delivery for large studies, ensuring compliance with regulatory standards. The position involves collaboration, stakeholder management, and quality maintenance, requiring robust project management skills and relevant experience.

Formación

• Typically 3-5 years of relevant experience.
• 7+ years of clinical research/monitoring experience or equivalent.
• Broad protocol and therapeutic knowledge.

Responsabilidades

• Ensure clinical delivery of assigned projects in compliance with regulatory requirements.
• Manage clinical aspects of projects, including scope and changes.
• Conduct team meetings, provide feedback, and support professional development.

Conocimientos

Project management practices

GCP knowledge

Clinical research knowledge

Communication

Educación

Bachelor's degree in healthcare or a scientific discipline

Descripción del empleo

Senior Global Trial Managers (SGTMs) are integral to clinical trial delivery, leading and collaborating with clinical teams to bring new drugs to market efficiently. SGTMs are part of the core project team responsible for the clinical delivery of large, multi-regional studies, ensuring compliance with contractual, SOP, policies, and practices. They oversee clinical delivery by leading teams and partnering with other functional groups to meet project requirements.

Responsibilities

Essential Functions:

• Ensure clinical delivery of assigned projects in compliance with regulatory requirements (ICH-GCP), protocol, customer requirements (contract), and internal policies (SOPs, project plans).
• Meet project clinical targets and contribute to risk mitigation planning throughout the project lifecycle.
• Maintain clinical quality by setting standards, measuring compliance, and managing quality issues.
• Manage clinical aspects of projects, including scope, changes, and out-of-scope work through Change in Scope (CIS) processes.
• Serve as the primary contact for the customer project manager.
• Identify and manage internal and external clinical stakeholders through effective communication.
• Support milestone achievement by collaborating with clinical teams and reporting to stakeholders.
• Manage resource and talent planning for clinical teams, including operational planning and training.
• Conduct team meetings, provide feedback, and support professional development.
• Adopt and promote corporate initiatives and changes.
• Contribute to clinical delivery strategies, participate in business proposals, and develop clinical operation plans.
• Mentor and coach new team members and support site visits as needed.

Requirements

• Typically 3-5 years of relevant experience.
• Bachelor’s degree in healthcare or a scientific discipline.
• 7+ years of clinical research/monitoring experience or equivalent.
• Knowledge of project management practices and terminology.
• Understanding of GCP, ICH guidelines, and clinical research industry standards.
• Broad protocol and therapeutic knowledge.
• Understanding of industry environments and project finances.

This position is not eligible for UK VISA Sponsorship

IQVIA provides clinical research services, insights, and healthcare intelligence to accelerate medical development and improve patient outcomes worldwide. We value diversity, inclusion, and belonging, fostering a culture that empowers innovation and collaboration.

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