Global Study Associate

AstraZeneca

Clinical study coordination
Electronic trial master file management
Regulatory document management
The Global Study Associate supports delivery of global clinical studies from study set-up through maintenance, close-out and study archiving in accordance with applicable clinical trial regulations and company policies

Job Summary

  • The Global Study Associate supports delivery of global clinical studies from study set-up through maintenance, close-out and study archiving in accordance with applicable clinical trial regulations and company policies.
  • This role involves coordinating activities with the Global Study Director, Associate Director, and Study Manager to ensure quality, consistency, and compliance across multiple studies and delivery models.
  • AstraZeneca offers an inclusive environment with global career growth opportunities, balancing in-person work with individual flexibility and a commitment to diversity and equality.

Matching Summary

The Global Study Associate supports delivery of global clinical studies from study set-up through maintenance, close-out and study archiving in accordance with applicable clinical trial regulations and company policies.

Skills & Requirements

Must-have

  • clinical study coordination
  • electronic Trial Master File management
  • regulatory document management
  • clinical trial compliance
  • study budget tracking
  • vendor oversight
  • meeting coordination and support

Nice-to-have

  • process improvement projects
  • cross-functional collaboration
  • digitalization and Lean processes
  • effective communication skills
  • administrative and logistical support

Key Requirements

  • Education in medical or biological sciences
  • Experience in clinical research administration
  • Proven organizational and analytical skills
  • Computer proficiency
  • Compliance with ICH-GCP and SOPs

Work Rights

Not specified

Tailored Resume

Cover Letter