Clinical Study Administrator For Biopharma Department

Zse68

Ich-gcp compliance
Etmf/isf management
Regulatory document submission
The Clinical Study Administrator supports the coordination and administration of interventional clinical studies from start-up through execution to close-out within the Local Study Team

Job Summary

  • The Clinical Study Administrator supports the coordination and administration of interventional clinical studies from start-up through execution to close-out within the Local Study Team.
  • The role ensures quality, consistency, and inspection readiness of study deliverables to meet time, cost, and quality objectives.
  • AstraZeneca embraces diversity and equality of opportunity and is committed to building an inclusive and diverse team.

Matching Summary

The Clinical Study Administrator supports the coordination and administration of interventional clinical studies from start-up through execution to close-out within the Local Study Team.

Skills & Requirements

Must-have

  • ICH-GCP compliance
  • eTMF/ISF management
  • Regulatory document submission
  • Clinical trial documentation
  • Study coordination and administration

Nice-to-have

  • Teamwork and communication skills
  • International environment experience
  • Proactive task efficiency improvement

Key Requirements

  • High school qualification
  • Administrative experience
  • Clinical process knowledge
  • Computer proficiency
  • Organizational capabilities
  • Good spoken and written English

Work Rights

Not specified

Tailored Resume

Cover Letter