CASUAL UNBLINDED STUDY COORDINATOR

Be part of the next generation of clinical research

Momentum Clinical Research operates a leading clinical trial network across Australia and New Zealand. With us, you’ll contribute to meaningful research that advances treatment options within a team that values quality, collaboration and enjoying the work we do.

The Opportunity

We are seeking a Registered Nurse to provide casual unblinded support for later-phase clinical trials.

This role primarily supports scheduled participant visits requiring the preparation, handling and dispensing of investigational product (IP). Your accuracy, clinical judgement and attention to detail will be essential to maintaining participant safety, study integrity and protocol compliance.

Work will be offered on an as-needed basis, with additional study coordination and clinical support undertaken where required.

About the Role

In this role, you will:

• Act as an unblinded member of the study team for nominated clinical trials.

• Prepare, reconstitute, calculate and dispense investigational product in accordance with study protocols, pharmacy/IP manuals and study-specific instructions.

• Verify participant, study, randomisation and treatment details before preparing or dispensing IP.

• Complete accurate dose calculations and independent checks where required.

• Maintain IP preparation, dispensing, accountability and reconciliation documentation.

• Ensure appropriate IP storage, handling and temperature requirements are maintained.

• Protect study integrity by maintaining clear separation between blinded and unblinded activities.

• Promptly escalate discrepancies, temperature excursions, preparation errors, protocol deviations and safety concerns.

• Support scheduled participant visits and complete clinical procedures within your professional scope, demonstrated competency and study delegation.

• Complete source documentation and study records accurately and contemporaneously.

• Assist with sponsor queries, monitoring visits and IP-related documentation queries where required.

About You

You’ll bring:

• A current qualification and registration to practice as a Registered Nurse in New Zealand.

• Demonstrated competency in medication preparation and administration.

• The ability to complete medication and dose calculations accurately.

• Strong attention to detail and the ability to follow detailed protocols and written instructions.

• Excellent documentation, organisation and time-management skills.

• Sound clinical judgement and the ability to recognise when escalation is required.

• Clear communication and a collaborative approach.

• Reliable and flexible availability for scheduled participant visits.

• Professionalism, confidentiality and the ability to strictly maintain study blinding.

Ideally, you’ll also have:

• Previous clinical research or Study Coordinator experience.

• Experience working with investigational products or in clinical trials.

• Current Good Clinical Practice (GCP) training.

• Experience preparing, reconstituting or dispensing injectable medications.

• Experience working within blinded clinical trials or as an unblinded study team member.

What We Offer

• Flexible casual work aligned with participant visits and study requirements.

• The opportunity to use your clinical skills in meaningful research.

• Study-specific training and clear procedures to support high-quality work.

• A collaborative and inclusive multidisciplinary team.

• The opportunity to contribute to better treatment options for patients.

How to Apply

If this sounds like a good fit, we’d love to hear from you. Apply through SEEK with your CV and a brief cover letter outlining your relevant clinical, medication preparation and clinical research experience.