At Momentum Clinical Research, we are reshaping the future of healthcare by conducting innovative clinical trials that enrich lives and improve global health outcomes. With over 20 years of experience and 14 purpose-built research sites across Australia and New Zealand, we are Australasia’s largest clinical trial network.

Formed from the union of three respected research organisations—AusTrials, P3 Research, and Holdsworth House Research—Momentum brings together deep expertise, a collaborative spirit, and a commitment to excellence. We pride ourselves on the quality of our research.

Due to continued growth and an expanding portfolio of clinical trials, we are seeking a skilled and detail-oriented Pharmacy Technician with clinical trial experience to join our team. In this role, you will work closely alongside our experienced IP Technician, supporting the management of investigational products across a variety of studies. This is a great opportunity to collaborate, learn, and contribute to meaningful research in a dynamic and supportive environment.

Key Responsibilities

Prepare, dispense, and manage investigational products in accordance with study protocols, GCP, and GMP standards

Maintain accurate pharmacy documentation, including IP accountability logs, temperature records, and inventory tracking

Collaborate with clinical and research teams to ensure timely and compliant IP handling

Support study start-up, closeout, and audit readiness from a pharmacy perspective

Participate in internal and external audits and inspections as required

Essential Qualifications & Experience

Minimum 1–2 years of experience working in a clinical trials setting or with investigational drugs

Strong understanding of ICH-GCP, TGA, and/or FDA / European regulatory requirements

Experience with IP accountability, randomisation systems (e.g., IWRS/IVRS), and temperature monitoring

Excellent attention to detail, organisational, and communication skills

Ability to work independently and collaboratively in a fast-paced research environment.

Desirable

Familiarity with electronic data capture (EDC) systems and clinical trial management systems (CTMS)

How to Apply

Please submit your CV with a cover letter outlining your relevant experience, expected salary, preferred working hours/days and when you would likely be able to start.