About Us:
Slade Health is a division of ICON Group. Slade Health is a national sterile compounding service provider with TGA accredited manufacturing facilities based in Queensland, Victoria and New South Wales. Slade Health is a trusted compounding partner in the clinical trial space, specialising in the aseptic preparation, management and secure delivery of investigational products for Phase I – IV clinical trials. To date, we have supported more than 700 clinical trials in Australia and 70 in New Zealand.
About the role:
We are seeking a Clinical Trials Pharmacist or suitably experienced Clinical Trials Specialist to join our established team at Mt Kuring-gai.
This role supports the GMP-compliant handling and oversight of Investigational Products (IP) prepared within our TGA-licensed sterile compounding facility. The position reports to the Clinical Trials Manager. This is a manufacturing and compliance-focused role within a regulated environment. It does not involve patient counselling or clinical dispensing.
This role will also align with operational needs and may require late finishes (up to 8pm) and minimal on-call responsibilities.
This position is suitable for:
- A registered Pharmacist with experience in sterile compounding or hospital pharmacy; or
- An experienced GMP or clinical trials professional with demonstrated capability in regulated environments.
Key Responsibilities:
- Manage investigational product inventory and accountability records
- Interpret trial protocols, pharmacy manuals, and sponsor instructions to ensure compliant IP preparation
- Maintain study documentation in alignment with ICH-GCP and GMP requirements
- Liaise with sponsors, CROs, and internal production teams
- Support oversight of clinical trial batch preparation within the sterile manufacturing environment
- Identify, document, and manage deviations, complaints, and CAPAs within the Quality Management System
- Contribute to process improvement and risk mitigation initiatives
- Maintain inspection readiness for sponsor and regulatory audits
- Build and maintain strong sponsor and stakeholder relationships
What We Are Looking For:
Essential (All Applicants)
- Strong organisational and documentation skills
- Experience working in a regulated environment (GMP, TGA, Medsafe, hospital pharmacy, or similar)
- High attention to detail and risk awareness
- Ability to manage competing priorities
- Strong communication skills and stakeholder engagement
Additional Requirements – Pharmacist Applicants
- Current AHPRA registration
- Experience in sterile compounding and/or hospital pharmacy highly regarded
Additional Requirements – Non-Pharmacist Applicants
- Tertiary qualification in science, pharmacy, biomedical science, or related discipline (or equivalent experience)
- Demonstrated experience in clinical trials operations, GMP manufacturing, or regulated quality systems
- Knowledge of Annex 13 or TGA manufacturing expectations highly regarded
How to Apply:
Have you ticked all of the above boxes? Are you ready for a new challenge? If you think you have the qualities we are looking for, then we want to hear from you!
If you meet the above criteria, please apply by clicking on the Apply Now button. Please attach a cover letter and resume when submitting your application. For further information about the role please contact Kimberly Soriano at [email protected].
Applications Close: 13th March 2026
Icon Group celebrates diversity and is committed to creating an inclusive workplace for all employees. We encourage applications from all diverse backgrounds.
Icon is committed to managing the risk of transmission of specified vaccine preventable diseases (VPDs). Certain roles may require the successful candidate to show evidence that they have been vaccinated against or are not susceptible to specified VPDs.