Clinical Trials Pharmacist

About the role

Join a fast‑paced clinical research pharmacy team that supports early‑phase and healthy‑volunteer studies. As a Clinical Trials Pharmacist you will manage investigational products, ensure compliant pharmacy operations and contribute to the successful delivery of clinical trials.

Key responsibilities

• Receive, store, monitor temperature, dispense, account for and destroy investigational products.
• Prepare sterile and non‑sterile investigational products, including compounding and small‑batch manufacturing.
• Maintain clean‑room standards, calibrate assets and perform environmental monitoring.
• Provide dosing, interaction, administration and storage guidance to study teams.
• Support study start‑up, documentation, monitoring visits and communication with medical staff.
• Manage stock, ordering and supply readiness for all study activities.
• Train staff in IP handling, dispensing and documentation.
• Work as an unblinded team member while preserving study blinding.
• Uphold ICH‑GCP, GMP and GDP principles with meticulous documentation.
• Participate in weekend/evening rosters and site‑based operational activities.

Required profile

• Bachelor of Pharmacy (or equivalent) with current AHPRA registration.
• At least 2 years experience as a registered pharmacist.
• Strong attention to detail, reliable judgement and excellent communication skills.
• Ability to work accurately in a time‑critical, regulated environment.
• Solid computer literacy and high‑quality documentation skills.
• Comfortable working independently and within multidisciplinary teams.

Required skills

• Investigational product management
• Sterile and non‑sterile compounding
• Clean‑room operation
• Temperature monitoring
• GMP compliance
• ICH‑GCP knowledge