Novatrials
Clinical Trial Coordinator
Skills
19 days ago
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Important information
Contract type:
Permanent
Salary:
A$93,600 / year
Location:
Charlestown NSW 2290, Australia
Work mode:
Onsite
Published on:
8 October 2026
What they need
About Novatrials
Novatrials is a leading private clinical trial centre dedicated to bringing new treatments and medical innovations to the Newcastle community. Since 2018, we have successfully delivered Phase I-IV clinical trials across a broad range of therapeutic areas, providing participants with access to cutting-edge therapies while supporting the advancement of medical science.
The Role
As a Clinical Trial Coordinator (CTC), you will be responsible for conducting clinical trials in compliance with study protocols, ICH-GCP, Novatrial SOPs, and relevant regulations and privacy laws.
Key responsibilities
- Assist with the effective and timely management of clinical trials activities including scheduling of participant appointments
- Assist with the identification and recruitment of participants into trials
- Implement and monitor study protocols and associated procedures
- Accurate data collection and entry of study data onto Case Report Forms and electronic clinical trial management system
- Manage and maintain study related documentation
- Perform participant assessments as required by the protocol
- Conduct questionnaires on participant reported outcomes
- Collection and preparation of human biological samples
- Maintain compliance with regulatory standards and ethical guidelines
About you
- Tertiary qualifications in a health-related field such as nursing, science, allied health, pharmacy, public health, and participant management experience
- Highly developed project planning, organisation, and time management skills with an ability to achieve, and/or exceed, key project milestones
- Demonstrated effective interpersonal, verbal, and written communication skills, interacting professionally with a variety of stakeholders
- High level of initiative and flexibility and the ability to meet deadlines while balancing multiple priorities
- Demonstrated ability to work competently in periods of high demand and activity
- Strong computer literacy skills using MS Office suite, database management and other online systems such as Clinical Trials Management Software
Desirables
- Venepuncture, IV cannulation and ECG skills
- Knowledge of Good Clinical Practice and applicable state and national laws, regulations guidelines
- Current driver's licence
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