Laboratory Assistant

**The Role**

The Laboratory Assistant in the Clinical Trial Oncology Unit will provide essential support to clinical research activities by assisting with sample collection, processing, storage, and documentation. The role ensures compliance with protocols and regulatory requirements while maintaining the highest standards of laboratory safety and efficiency.

**Key responsibilities**:

- Assist in the collection, labelling, and processing of biological samples (e.g., blood, tissue, urine) in accordance with study protocols.
- Prepare and maintain laboratory equipment and workspaces, ensuring compliance with Good Laboratory Practices (GLP).
- Support the storage, handling, and shipment of clinical trial specimens following regulatory guidelines.
- Maintain accurate and organised laboratory records, logs, and documentation for quality control and regulatory compliance.
- Perform routine laboratory tasks, including centrifugation, and reagent preparation.
- Assist in quality assurance procedures to ensure the integrity and reliability of sample processing.
- Adhere to biosafety and infection control protocols in accordance with institutional and regulatory standards.
- Coordinate with clinical and research teams to facilitate seamless laboratory operations.
- Manage laboratory inventory, ordering supplies as needed.
- Manage the kit room, ensuring all equipment and materials are stored properly and in an organized manner.
- Maintain a clean and orderly kit room environment, following all safety and storage protocols.
- Participate in training sessions and continuing education to stay updated on best practices and new technologies.

**Selection Criteria**
- Bachelor’s degree or diploma in a relevant scientific field (e.g., Biology, Medical Laboratory Science, Biotechnology) preferred.
- Previous experience in a clinical or research laboratory setting, preferably in oncology or clinical trials.
- Knowledge of biospecimen handling, processing techniques, and laboratory safety regulations.
- Familiarity with Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) guidelines.
- Strong organisational and data management skills with attention to detail.
- Ability to work collaboratively in a fast-paced research environment.
- Strong communication and problem-solving skills.

**Benefits**
- Optional NFP salary packaging - increase your take home pay with $15,900 tax free benefit + meal and entertainment card.
- Fitness Passport Access.
- Employee Assistance program.
- Onsite gym.
- Access to e-learning programs and an opportunity to progress your career.

**Culture**

At Chris O’Brien Lifehouse, we are committed to providing a working environment where each individual is valued, respected, and supported to progress. Our priority is to ensure culture, policies, and processes are truly inclusive and that no one is disadvantaged on the basis of their Aboriginal and Torres Strait Islander identity, gender, culture, disability, LGBTIQA+ identities, family and caring responsibilities, age, or religion. We encourage everyone who meets the selection criteria and shares Chris O'Brien Lifehouse values to apply.