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Study Manager

2 months ago

London, Greater London, United Kingdom IQVIA Full time

Job Overview:

As a Clinical Project Manager at IQVIA, you will be responsible for leading the operational aspects of clinical trials from study start-up to close-out. You will act as the primary point of contact to manage and coordinate the conduct of clinical trials in accordance with ICH-GCP and other applicable local regulations.

Key Responsibilities:

  • Partner with global and local country teams to provide high-level country strategy and drive study progress.
  • Plan, manage, and maintain oversight of clinical study execution in accordance with the global program strategy.
  • Support country-level operational planning and be accountable for site selection within assigned countries.
  • Contribute to the development of program and study-specific materials.
  • Oversight and monitoring of applicable vendor activities.
  • Monitor the execution of the clinical study against timelines, deliverables, and budget.

Requirements:

  • Bachelor's degree in a healthcare or other scientific discipline.
  • Clinical monitoring experience required.
  • Minimum 2-3 years' experience of leading local/regional or global teams.
  • Minimum 2-3 years' clinical trial project management experience.
  • Clinical trial processes and operations.
  • Extensive knowledge of ICH/GCP regulations and guidelines.
  • Project and program management, including oversight of study deliverables, budgets, and timelines.
  • Time, cost, and quality metrics, Key Performance Indicators (KPIs).

What We Offer:

  • Remote working options.
  • The opportunity to work on cutting-edge medicines at the forefront of new medicines development.
  • Access to significant data pools for better site selection and recruitment.
  • Genuine career development opportunities for those who want to grow with the organization.