Clinical Trials Coordinator – Oncology Research & Care

Mylifehouse; Sydney; On-site; AUD 70,000 - 90,000; Full time

Benefits offered by this job

NFP salary packaging

Fitness Passport Access

Employee Assistance program

Onsite gym

Access to e-learning programs

Job summary

Chris O’Brien Lifehouse is seeking a Clinical Trials Study Coordinator to support the Medical Oncology Department in delivering high‑quality, patient‑centred trial care. You will coordinate trial operations, maintain documentation, and ensure adherence to protocols while communicating with investigators and sponsors.

Ideal candidates bring a science or health care degree and at least 1 year of study coordination experience, with confidentiality and privacy at the forefront.

Qualifications

• Degree in science or a health care discipline.
• Minimum 1 year of experience as a Study Coordinator.
• Ability to maintain confidentiality and privacy.
• Desirable: EDC systems experience (iMedidata RAVE, InForm).
• Desirable: Medical oncology knowledge.

Responsibilities

• Coordinating all aspects of clinical trial operations, ensuring regulatory compliance and study protocols.
• Facilitating communication between investigators, sponsors, and other stakeholders.
• Overseeing patient recruitment, screening, and enrolment processes.
• Maintaining accurate and up-to-date study documentation and data management.
• Monitoring and reporting adverse events and protocol deviations.
• Providing exceptional support and guidance to study participants throughout the trial process.

Skills

Study coordination

Clinical research

Communication

Confidentiality

Education

Degree in science or health care

Tools

iMedidata RAVE

InForm

Job description

Chris O’Brien Lifehouse is seeking a Clinical Trials Study Coordinator to support the Medical Oncology Department in delivering high‑quality, patient‑centred trial care. You will coordinate trial operations, maintain documentation, and ensure adherence to protocols while communicating with investigators and sponsors.

Ideal candidates bring a science or health care degree and at least 1 year of study coordination experience, with confidentiality and privacy at the forefront.