Clinical Trials Assistant (contract)

ResMed

Sydney, Australia
On-site
Support clinical development and trials
Prepare study devices and materials
Manage clinical study database and crfs
The Medical Affairs team collaborates with leaders to ensure clinical research aligns with strategic priorities and maintains global compliance

Job Summary

  • The Medical Affairs team collaborates with leaders to ensure clinical research aligns with strategic priorities and maintains global compliance.
  • As a Clinical Trials Assistant, you will support Clinical Development Specialists and Medical Affairs Management in product development and clinical trial planning.
  • This role involves preparing study materials, managing databases, monitoring data, assisting with audits, and archiving study documentation.

Matching Summary

The Medical Affairs team collaborates with leaders to ensure clinical research aligns with strategic priorities and maintains global compliance.

Skills & Requirements

Must-have

  • Support clinical development and trials
  • Prepare study devices and materials
  • Manage clinical study database and CRFs
  • Monitor clinical study data compliance
  • Assist with audits and inspections
  • Document and archive study data

Nice-to-have

  • Develop stakeholder relationships
  • Follow standard practices and procedures
  • Receive guidance and direction

Key Requirements

  • Bachelor’s degree in relevant studies
  • Ability to prioritize multiple tasks
  • Proficient in Outlook, Word, Excel, PowerPoint
  • Previous experience in clinical studies (preferred)
  • Knowledge of GCP and ISO 14155 (preferred)

Work Rights

Not specified

Tailored Resume

Cover Letter