Hiring Clinical Research Associates & Coordinators

We’re Hiring!

Experienced CRCs & CRAs
**Study/Clinical Research Coordinators/ CRA I / CRA II / Senior CRAs

Relocate to Brisbane and Advance Your Clinical Research Career

Company: Thermo Fisher Scientific
Location Specific: #Brisbane #Queensland #Australia
Work set-up: #Remote

Key Responsibilities
- Perform and coordinate all aspects of clinical monitoring and site management, including:
- Source Data Review (SDR) and Source Data Verification (SDV)
- Preparation of visit reports
- Maintenance of accurate and compliant study documentation
- Identification and resolution of site issues and action items
- Conduct on-site and remote monitoring visits to ensure protocol and regulatory compliance
- Ensure studies are conducted in accordance with ICH-GCP, regulatory requirements, and SOPs, safeguarding subject safety and data integrity
- Maintain audit readiness at all times
- Build strong, collaborative relationships with investigational sites
- Partner cross-functionally with Clinical Trial Managers, Study Start-Up, and Regulatory teams

What We’re Looking For
- Currently based in Australia or New Zealand, with confirmed plans or readiness to relocate to Brisbane ( Relocation support to Brisbane may be provided for the successful candidate )
- Minimum 5+ years’ experience as a Clinical Study/Research Coordinator (sponsor-driven trials), or 6–12 months’ experience as a CRA
- Bachelor’s degree in life sciences, nursing, or related field
- Solid understanding of clinical trials and ICH-GCP guidelines
- Ability and willingness to travel extensively (70–80%)
- Valid Australian/New Zealand driver’s license
- Australian or New Zealand citizen, or Australian permanent resident

If you're interested or know someone who might be, feel free to send the resume to me so I can refer

Email: joan.mallari@thermofisher.com

Thanks!