Clinical Trial Research Support

chas.uni.edu

Unknown, Unknown, Unknown
Base: $112, 628 (pro rata); bonus/equity: not spec...
Ich-gcp guidelines knowledge
Ethics and regulatory compliance
Data management and reporting
This role will support trial operations from start-up to closeout, including ethics and regulatory submissions, site coordination, data management, and monitoring

Job Summary

  • This role will support trial operations from start-up to closeout, including ethics and regulatory submissions, site coordination, data management, and monitoring.
  • Key responsibilities include designing and adapting clinical trial procedures, planning trial timelines, monitoring progress, and ensuring ethical and regulatory compliance.
  • The University of Sydney is committed to creating a diverse and inclusive community and welcomes applications from all backgrounds.

Matching Summary

This role will support trial operations from start-up to closeout, including ethics and regulatory submissions, site coordination, data management, and monitoring.

Salary

Base: $112, 628 (PRO RATA); Bonus/Equity: Not specified; Benefits: 17% superannuation

Skills & Requirements

Must-have

  • ICH-GCP guidelines knowledge
  • Ethics and regulatory compliance
  • Data management and reporting
  • Trial operations support
  • Site coordination and monitoring

Nice-to-have

  • Team leadership and performance management
  • Continuous improvement initiatives
  • Promote safe and inclusive environment
  • Effective collaboration with stakeholders

Key Requirements

  • Unrestricted work rights in Australia
  • Sound knowledge of ICH-GCP guidelines
  • Knowledge of ethical and regulatory requirements
  • Knowledge of confidentiality and privacy laws

Work Rights

Unrestricted work rights in Australia

Tailored Resume

Cover Letter