Oncology Clinical Trials Coordinator

St Vincent's Health Australia; Sydney; On-site; AUD 82,000 - 121,000; Full time

Benefits offered by this job

Competitive pay packaging

World-class precinct

Study leave & scholarships

Fitness Passport & health benefits

Career development

NSW Health transfer benefits

Job summary

St Vincent's Health Australia in Sydney seeks a Clinical Trial Coordinator/Registered Nurse to manage and deliver patient-centred cancer trials at The Kinghorn Cancer Centre. You will work within a multidisciplinary team to ensure protocol adherence and high-quality study conduct.

The role requires RN (Division 1) with AHPRA and experience in clinical trials or related qualifications, plus strong data management and communication skills.

Qualifications

• Currently registered as a Registered Nurse (Division 1) with the Australian Health Practitioner Regulation Agency.
• Holds or is working towards qualifications in clinical research / clinical trials or equivalent experience.
• Demonstrated leadership in a team and ability to use own initiative.
• Experience with secure data management and HREC/RGO submissions.
• RN in clinical trials with knowledge of oncology/haematology and research principles.

Responsibilities

• Coordinate and deliver high-quality, patient-centred clinical trials within The Kinghorn Cancer Centre.
• Support safe conduct of research per study protocols, ICH-GCP, and regulatory requirements.
• Screen participants, coordinate visits and trial schedules, and manage data and samples.
• Communicate with patients, families, healthcare professionals, sponsors and partners; contribute to quality improvement.

Skills

Clinical research

Registered Nurse

Team leadership

Time management

Data management

Education

RN Registration

Clinical trials qual

Tools

GCP

Job description

St Vincent's Health Australia in Sydney seeks a Clinical Trial Coordinator/Registered Nurse to manage and deliver patient-centred cancer trials at The Kinghorn Cancer Centre. You will work within a multidisciplinary team to ensure protocol adherence and high-quality study conduct.

The role requires RN (Division 1) with AHPRA and experience in clinical trials or related qualifications, plus strong data management and communication skills.