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Clinical Trial Coordinator

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Onsite

Clinical Trial Coordinator

Novatrials

Clinical Trial Coordinator

Skills

Google Cloud PlatformCompliance

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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