Senior Global Clinical Trial Delivery Lead

IQVIA

Paris

Sur place

EUR 90 000 - 140 000

Plein temps

Il y a 9 jours
Générateur de candidature

Une candidature sur mesure pour ce poste — un CV personnalisé et une lettre de motivation qui correspondent directement à l’offre.

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Résumé du poste

IQVIA in Paris is seeking a Senior Clinical Trial Manager to lead the Study Management Team, oversee trial planning from start-up through close-out, and ensure real-time reporting and inspection readiness.

You will coordinate with country and regional staff, manage budgets and vendor activities, and drive CAPAs and risk mitigation in a global, virtual environment. Travel is required and effective cross-functional communication is essential.

Qualifications

  • BS degree or equivalent in Life Sciences.
  • 6-8 years clinical trial management experience in pharma/CRO.
  • Strong working knowledge of ICH-GCP, local laws and regulations.
  • Proven leadership to drive Study Management Team through trial stages.
  • Experience coordinating global/regional teams in virtual environments.
  • Proficient in English and local language.

Responsabilités

  • Lead the Study Management Team, providing updates on deliverable status.
  • Ensure real-time trial status reporting and inspection readiness.
  • Manage documentation and communication of trial progress.
  • Coordinate with country/regional staff and Global Trial Lead.
  • Oversee CAPAs and issue resolution; drive risk mitigation.
  • Support site selection, feasibility, and enrollment planning.
  • Oversee budgets, vendor selection, invoices, and spend.
  • Develop and maintain trial-specific training materials and records.

Connaissances

Leadership
CDM coordination
Budgeting
ICH-GCP knowledge
Vendor management
Communication

Formation

BS degree in Life Sciences

Outils

Trial Master File
CTMS

Description du poste

IQVIA in Paris is seeking a Senior Clinical Trial Manager to lead the Study Management Team, oversee trial planning from start-up through close-out, and ensure real-time reporting and inspection readiness.

You will coordinate with country and regional staff, manage budgets and vendor activities, and drive CAPAs and risk mitigation in a global, virtual environment. Travel is required and effective cross-functional communication is essential.

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