Position Overview
Clinical Research Assistant – Cardio‐Oncology (12‐month fixed term, up to July 2027)
Key Responsibilities
* Assist with human research ethics committee (HREC) and governance applications, submissions & amendments, with guidance from oncologists, cardiologists, and the wider research team.
* Assist with patient identification and recruitment, ensuring informed consent is obtained, information is provided, and study protocols are adhered to.
* Schedule patient visits for study procedures and follow‐up.
* Conduct clinical assessments, including medical history and organising sample collection.
* Monitor patient safety and provide ongoing education and support to study participants.
* Accurately record clinical and research data in electronic and paper‐based systems.
* Maintain study databases and prepare reports and regulatory documentation.
Essential Criteria – You will have:
* Relevant qualification with a minimum of 2 years' experience in clinical research or a related field.
* Experience in the preparation and submission of ethics applications and knowledge of Good Clinical Practice (GCP) and research governance requirements.
* Experience with patient recruitment, informed consent, and clinical trial coordination.
* Strong clinical skills with proven ability to manage high‐level patient interactions and translate technical procedural details into accessible language for the informed consent process.
* Proficiency in data collection and electronic medical records (EMR) systems.
* Commitment to patient safety and ethical research practices.
* Ability to work independently and as part of a team.
* High attention to detail and accuracy in data collection and reporting.
* Excellent interpersonal skills and ability to work collaboratively with a range of health professionals and researchers.
* Excellent communication and organisational skills.
Desirable Criteria – You will have:
* Postgraduate qualification in clinical research, public health, or a related field.
* Experience in a relevant specific speciality area (e.g., oncology, cardiology, imaging).
* Familiarity with regulatory requirements such as the Therapeutic Goods Administration (TGA) and Human Research Ethics Committees (HREC).
What We Offer
* An opportunity to be part of an exciting new research project.
* Outstanding opportunity to work in a world‐class research and education precinct.
* A supportive team and collaborative work environment.
Additional Information
The position is a Category A appointment under the NSW Health Policy – applicants must provide evidence of protection against specified infectious diseases at their own cost prior to appointment.
To apply you must hold an appropriate Australian or New Zealand work visa.
Equal Employment Opportunity
The Heart Research Institute supports Equal Employment Opportunity.
We value diversity and encourage applications from women, Aboriginal and Torres Strait Islanders, Māori and Pasifika peoples, people with disability, LGBTQI individuals and applicants of diverse cultures and ages.
We are committed to the safety and wellbeing of our employees and affiliates, and our community. Whoever you are, you are welcome at HRI.
If you have a disability and need support to submit your application, please email support@example.com.
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