Clinical Trials Coordinator

CREDO (Centre for Research and Education in Diabetes and Obesity) continues to grow and thrive, enabling another exciting opportunity for a Clinical Trial Coordinator to join the team in a part-time or full-time fixed term position. We are seeking someone to work with for 24hours/week.

The successful applicant will become part of an established team and will be responsible for the primary coordination of clinical trials and the management of patients on those trials. The role involves delivery of direct and in-direct clinical-trial-related care of patients, associated data collection and maintenance of essential trial document for concurrent studies.

A regular day will see you:

Coordinate and manage a number of trials concurrently

Manage the care of patients participating in clinical trials, ensuring compliance with the trial protocol, reporting requirements and ICH-GCP guidelines

Ensure accurate and timely source documentation and data entry, and the maintenance of essential documents that validate integrity in the conduct of the clinical trial

Liaise with Principal Investigators, multidisciplinary team and Trial Monitors

You will be someone who has excellent communication skills, with a strong commitment to excellence in patient care. You’ll bring energy and drive to your work, and have a keen interest in developing your skillset.

The atmosphere within CREDO is energetic, friendly and cohesive, with a strong teamwork ethic amongst all members. We have a strong focus on continual improvement and professional development.

If you are a Registered Nurse (Div 1) or hold a degree in a relevant field with clinical trial coordination experience, enjoy being part of a dynamic team and have a positive attitude, we look forward to your application today.

To be successful in this role you’ll bring with you:

Registered Nurse (Division 1) with current AHPRA registration or a degree in a relevant field

Awareness of ICH-GCP Guidelines and relevant regulatory guidelines.

Excellent team working skills, with ability to work independently

Enthusiasm, willingness to learn and contribute to the research team.

Developed computer literacy skills and familiarity with Office 365

We are committed to cultural safety and health equity for Aboriginal and/or Torres Strait Islander People. We celebrate, value, and include people of all backgrounds, genders, identities, cultures, bodies, and abilities. We welcome and support applications from talented people identifying as Aboriginal and/or Torres Strait Islander, people with disability, neurodiverse people, LGBTQIA+ and people of all ages and cultures.

If you feel this role is right for you, we encourage your early application. Even if you don’t meet every single requirement, we encourage you to apply. What matters most is your passion, your drive and your willingness to learn and contribute. Applications will be reviewed as they are received, and interviews may take place prior to the closing date. This means we reserve the right to close a job ad prior to the advertised closing date.

All appointments are made subject to a satisfactory National Police Check and if required, a Working With Children Check. Austin Health is a child safe organisation, committed to upholding the rights, safety, and wellbeing of children and young people in line with Child Safe Standards. If you require any reasonable adjustments to the recruitment process, you are welcome to reach out to the hiring manager: Adele Manzoney, Clinical Trial Manager, Adele.MANZONEY@austin.org.au