Location: Brisbane, Australia (Home-based, 100% remote)

Employment Type: Full-time

About the Role
Are you an experienced Clinical Research Coordinator ready to step into a Clinical Research Associate (CRA) role—or a newly appointed CRA looking to strengthen your monitoring skills? We are seeking motivated and detail-oriented professionals to join our CRA team in Queensland. This opportunity is ideal for CRCs looking to transition into monitoring, as well as junior CRAs who are early in their careers and eager to build a strong foundation.

Key Responsibilities

• Performs and coordinates all aspects of the clinical monitoring and site management process, including but not limited to: source data review (SDR) and verification (SDV), visit reports, maintain accurate study documentation, identify & address site issues and action items.
• Conducts on-site and remote site visits to assess protocol and regulatory compliance and manages required documentation.
• Ensure trials are conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability.
• Ensures audit readiness.
• Develops collaborative relationships with investigational sites.
• Collaborate with cross-functional teams, including Clinical Trial Managers, Study Start-Up and Regulatory teams

What We’re Looking For

• Minimum 5+ years’ experience as a Clinical Study/Research Coordinator working on sponsor-driven trials, or an early-career Clinical Research Associate (approximately 6–12 months’ experience)
• Bachelor’s degree in life sciences, nursing, or a related field
• Solid understanding of clinical trial processes and ICH-GCP guidelines
• Strong attention to detail, time management, and organisational skills
• Critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving
• Good oral and written communication skills, with the ability to communicate effectively with medical personnel
• Ability to work in a team or independently as required
• Strong computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software
• Strong English language and grammar skills
• Ability to remain flexible and adaptable in a wide range of scenarios
• Ability and willingness to travel extensively (approximately 70–80%)
• Valid Australian driver’s licence and ability to travel independently to sites
• Australian citizen or permanent resident only

What We Offer

• Structured CRA onboarding and training program tailored to your experience level
• Mentorship and clear progression pathway to independent CRA
• Exposure to a vast variety of clinical trials across different therapeutic areas and sponsors
• Competitive salary, car/travel allowance, and benefits
• Supportive and collaborative team culture

Why Join Us?
We recognise the value of both strong site experience and early CRA exposure. Whether you’re stepping up from a CRC role or building on your initial CRA experience, we provide the training, support, and opportunities to help you succeed and grow your career.