Clinical Research Associate
IQVIA · Melbourne, Australia +1 more
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
IQVIA seeks Clinical Research Associates for monitoring and site management roles across Australian locations. The position involves conducting study monitoring visits, managing site recruitment, ensuring protocol compliance, and maintaining regulatory documentation in accordance with GCP and ICH guidelines.
What they're looking for
- Bachelor's degree in scientific or healthcare discipline
- Minimum 9 months independent on-site monitoring experience
- Knowledge of GCP and ICH regulatory requirements
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Organizational and problem-solving skills
- Ability to establish effective working relationships with stakeholders
What you'll be doing
- Conduct site monitoring visits including initiation, ongoing monitoring, and close-out activities
- Work with sites to develop and track subject recruitment plans aligned with project timelines
- Train sites on protocol requirements and maintain regular communication on project expectations
- Evaluate site compliance with protocol and regulatory standards; escalate quality issues
- Track study progress including regulatory submissions, enrollment, CRF completion, and data queries
CompensationCompetitive salary with car and health allowances
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.