Clinical Research Assistant

4 weeks ago


Brisbane, Queensland, Australia QIMR Berghofer Full time

2 days ago Be among the first 25 applicants

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  • Gain hands-on experience in clinical trial coordination
  • Attractive salary packaging & superannuation options

    • Part-time opportunity
    • Gain hands-on experience in clinical trial coordination
    • Attractive salary packaging & superannuation options

    About QIMR Berghofer

    QIMR Berghofer is a world-leading translational medical research institute focused on improving health by developing new diagnostics, better treatments and prevention strategies, specifically in the areas of Cancer, Infection and Inflammation, Brain and Mental Health, and Population Health. Based in Herston, Brisbane and working in close collaboration with clinicians and other research institutes, QIMR Berghofer is home to more than 600 scientists, students and non-research staff.

    About Your Lab

    The Statistical Genetics laboratory at QIMR Berghofer comprises staff and students working on statistical methods development and on applications to data.

    The Statistical Genetics group develops and applies statistical methods to gene mapping studies across a wide range of traits and diseases. A major interest is ophthalmological genetics, with work ongoing to harness knowledge of the specific genes involved in eye disease to predict future disease risk and prevent blindness.

    Role Purpose / Responsibilities

    Applications are invited for a Clinical Research Assistant/ Nurse to play a vital role in the conduct of an investigator-initiated clinical trial, The Genetics of Glaucoma Trial. This clinical trial will investigate the effectiveness of determining frequency of eye examinations for glaucoma based on a person's estimated genetic risk, thereby providing evidence for more effective glaucoma monitoring in the Australian healthcare system in the future.

    Duties Include But Are Not Limited To
    • Assist in the conduct, consent process and coordination of clinical trial alongside research staff and clinicians
    • Data collation for a range of participant ocular assessments (e.g. visual fields, OCT imaging, intraocular pressure)
    • Support clinical procedures and data collection in accordance with trial protocols (training provided)
    • Manage patient scheduling, communication, and accurate data entry
    • Liaise with patients, optometrists, and healthcare staff to ensure smooth trial delivery

    About You

    To be successful in this role, you will have:
    • A tertiary qualification in Nursing, Orthoptics or relevant medically registered discipline
    • Basic knowledge of clinical assessments used in optometry such as visual fields, intraocular pressure and ocular imaging
    • High level interpersonal skills, including the ability to form productive professional relationships and communicate effectively with various stakeholders
    • Proven ability to build and maintain excellent rapport with a wide range of patients, ensuring effective and compassionate communication and care
    • Willingness and ability to quickly learn new techniques and procedures
    • Demonstrated proficiency in Microsoft Office Suite
    • A solutions-oriented approach with a commitment to working collaboratively with others and fostering a supportive team environment

    Desirable
    • Understanding of clinical trial processes with some knowledge and understanding of ethics, governance, privacy and ICH-GCP principles
    • Understanding of clinical genetic risk scores
    • Current GCP certification
    • Demonstrated ability using project tracking tools and systems related to research trials

    Remuneration: Salary range is $76,153 to $103,108 p.a (full-time equivalent ) plus super and generous salary packaging. This position is offered on a part-time, fixed-term basis for 2.5 years. The following part-time work arrangements will apply and the salary will be paid pro-rata accordingly:
    • 4 days per week (0.8 FTE) for the first 6 months
    • 2 days per week (0.4 FTE) for a further 2 years

    For further information: please contact Senior Group Leader, Stuart MacGregor via email Stuart.MacGregor@qimrb.edu.au

    Closing Date: Sunday, 3 August 2025

    To submit an application: use the APPLY button. All applicants must supply the following documents: Resume and Cover letter addressing the selection criteria outlined in the Position Description.

    Applicants must be an Australian Citizen, Permanent Resident or hold a valid work permit or visa. Work eligibility will be checked as part of the recruitment process.

    What We Offer
    • Salary Packaging
    • State of the art facilities
    • Stimulating work setting focussed on cutting edge medical research
    • Supportive and collaborative team environment
    • Parental Leave provisions
    Seniority level
    • Seniority levelEntry level
    Employment type
    • Employment typePart-time
    Job function
    • Job functionResearch, Analyst, and Information Technology
    • IndustriesResearch Services

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