Part-Time Oncology Clinical Research Coordinator

GenesisCare UK; St Leonards; On-site; AUD 60,000 - 90,000; Part time

Job summary

GenesisCare is seeking a part-time Clinical Research Coordinator to join the St Leonards clinic in the North Shore Health Hub. You will play a hands-on role in coordinating oncology clinical trials, ensuring GCP and regulatory compliance, and delivering high-quality patient care.

The ideal candidate holds a science or healthcare qualification with at least 12 months of hands-on CRC experience and is comfortable working across study start-up, recruitment, visits, monitoring, and close-out

Qualifications

• Minimum 12 months' experience as a Clinical Research Coordinator in oncology or clinical trials.
• Experience coordinating and delivering clinical trials from start-up to close-out.
• Strong understanding of GCP and regulatory requirements.

Responsibilities

• Support delivery of oncology clinical trials in line with protocols and regulatory requirements.
• Coordinate daily trial operations with investigators to maintain study momentum.
• Involve start-up, recruitment, patient visits, monitoring and close-out stages.
• Ensure study documentation and regulatory records are inspection-ready.
• Perform clinical procedures such as vitals, ECGs and venepuncture when trained.
• Provide a positive, professional experience for patients throughout their trial participation.
• Collaborate with internal teams, providers, and sponsors to keep studies running smoothly.
• Assist with site monitoring visits, audits, and compliance activities.
• Maintain training compliance and a culture of quality and continuous improvement.

Skills

Clinical trial coordination

GCP knowledge

Patient communication

Regulatory compliance

Trial lifecycle understanding

Education

Science/Healthcare qualification

Nursing qualification

Pharmacy qualification

Job description

GenesisCare is seeking a part-time Clinical Research Coordinator to join the St Leonards clinic in the North Shore Health Hub. You will play a hands-on role in coordinating oncology clinical trials, ensuring GCP and regulatory compliance, and delivering high-quality patient care.

The ideal candidate holds a science or healthcare qualification with at least 12 months of hands-on CRC experience and is comfortable working across study start-up, recruitment, visits, monitoring, and close-out