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Senior Global Trial Manager

Senior Global Trial Manager

IQVIAmadrid, España
Hace 16 días
Descripción del trabajo

Job Overview

Senior Global Trial Managers (SGTMs) are key contributors to clinical trial delivery, leading and collaborating with clinical teams to improve patient outcomes by expediting the development of new drugs. 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 to clients by managing clinical teams and coordinating with other functional teams to meet project requirements consistently.

Responsibilities

Essential Functions :

  • Ensure clinical delivery of assigned projects complies with regulatory standards (ICH-GCP), protocol, customer requirements (contract), and internal policies (SOPs, project plans).
  • Be accountable for achieving project clinical targets.
  • Contribute to developing and managing risk mitigation plans throughout the project lifecycle.
  • Maintain clinical quality by setting standards, measuring compliance, and overseeing quality issue management.
  • Manage clinical aspects of the project, including scope, planning, and change management (CIS process).
  • Serve as the primary contact for the customer project manager.
  • Identify and manage internal and external stakeholders through effective communication and resolution strategies.
  • Support milestone achievement by collaborating with the clinical team and reporting to stakeholders.
  • Plan and manage clinical team resources, including training and professional development.
  • Conduct team meetings and facilitate communication to meet objectives.
  • Support corporate initiatives and serve as a change advocate.
  • Contribute to clinical delivery strategy development, bid proposals, and project planning.
  • Mentor and coach new team members as needed.
  • Participate in site visits to support project delivery.

Requirements

  • Typically requires 3-5 years of relevant experience.
  • Bachelor’s degree in healthcare or a related scientific discipline.
  • 7+ years of clinical research / monitoring experience or equivalent.
  • Knowledge of project management practices and terminology.
  • Good understanding of GCP and ICH guidelines.
  • Broad protocol and therapeutic knowledge.
  • Understanding of the clinical research industry and operational environments.
  • Basic understanding of project finances and scope management.
  • This position is not eligible for UK VISA Sponsorship

    IQVIA is a leading provider of clinical research services, commercial insights, and healthcare intelligence, committed to accelerating medical innovation and improving patient outcomes worldwide. Learn more at

    We value diversity, inclusion, and belonging, fostering a culture that empowers our employees to innovate and collaborate, ultimately delivering better healthcare solutions globally.

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