Clinical Research Coordinator – Full-Time
Ready to step away from shift work and build a career in clinical trials? This is a fantastic opportunity for a Nurse or Pharmacist to transition into research within a supportive, high-performing clinical trials environment.
Join a collaborative site team delivering a diverse portfolio of studies across areas such as vaccines, dermatology, respiratory disease, diabetes, and more. This role offers a unique blend of clinical care and study coordination, with strong opportunities for professional growth and skill development.
About the Role
This is a full-time, site-based position (with flexibility for the right candidate), combining hands-on clinical responsibilities with study coordination duties.
Key Responsibilities
* Coordinating participants throughout clinical trials
* Administering and dispensing investigational products
* Ensuring compliance with protocols, GCP, and regulatory requirements
* Managing study documentation, source data, and CRFs
* Collaborating with investigators, ethics committees, and study teams
About You
* Registered Nurse or Pharmacist (AHPRA registered)
* Experience in vaccinations
* Strong communication skills and a collaborative mindset
* High attention to detail with excellent organisational skills
* Confident using clinical systems, databases, and EMRs
* Ability to manage multiple priorities and meet deadlines
* Proactive, adaptable, and solutions-focused
Desirable
* Experience in clinical trial coordination (commercial studies preferred)
* Knowledge of GCP, ethics, and regulatory requirements
* Experience with sample handling, processing, and shipping
Why Apply?
* Transition out of shift work into a structured, weekday role
* Gain hands‐on experience in clinical research
* Work within a supportive and growing clinical trials network
* Develop valuable skills across a wide range of therapeutic areas
If you're looking to diversify your career and step into the world of clinical research, this role offers the perfect entry point.
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