Clinical Research Coordinator - Oncology Research

Icon Group; City of Brisbane; On-site; AUD 65,000 - 90,000; Full time

Job summary

Icon Group's Icon Research unit in Brisbane is seeking a Clinical Research Coordinator to deliver oncology and haematology trials from start-up to close-out. You will work with investigators, research nurses and multidisciplinary teams to ensure high-quality, compliant trial delivery.

You'll coordinate complex portfolios, contribute to patient recruitment, and participate in site activation with ongoing professional development within Australia's largest clinical trial network.

Qualifications

• Experience coordinating clinical research studies, preferably in oncology/haematology.
• Strong organisational and time-management skills.
• Excellent communication and stakeholder management abilities.

Responsibilities

• Coordinate day-to-day running of oncology/haematology clinical trials.
• Support participant recruitment and guide participants through trial journeys.
• Collaborate with investigators, sponsors, monitors and other stakeholders.
• Coordinate study visits, assessments and trial procedures.
• Maintain study documentation and regulatory records.
• Assist with start-up activities to enable site activation.
• Ensure studies adhere to protocol, GCP and regulatory requirements.

Skills

Clinical research coordination

Oncology/haematology exposure

Organisational skills

Communication skills

Attention to detail

Team collaboration

Job description

Clinical Research Coordinator - Oncology Research

Join a team at the forefront of cancer research
Due to ongoing expansion of our clinical trials program, we are seeking interested clinical trial professionals to join our team.
This permanent full-time role will be based within our clinical trials unit at Icon Cancer Centre South Brisbane. Within the role you'll have the opportunity to work on innovative oncology and haematology clinical trials that are helping shape the future of cancer care.
As part of a highly experienced and supportive clinical trials team, you'll coordinate a diverse portfolio of studies in our fast-paced research unit. This role will see you working alongside leading investigators, research nurses and clinical trial professionals.
This is an opportunity to contribute to research that gives patients access to tomorrow's treatments today while building a rewarding career in one of Australia's largest clinical trial networks.
Whether you're an experienced Clinical Research Coordinator looking for your next challenge, or an oncology professional interested in transitioning into research, we'd love to hear from you.
Why Join us?
Work on studies that matter
Be part of a team delivering cutting‑edge oncology and haematology research that has a direct impact on patient outcomes.
Gain exposure to early phase clinical trials
Develop your experience working on complex and innovative studies within an established Phase 1 Oncology Unit.
Build your career
Access structured training, ongoing professional development and opportunities to progress within a growing national research network.

Join a team at the forefront of cancer research
Due to ongoing expansion of our clinical trials program, we are seeking interested clinical trial professionals to join our team.
This permanent full-time role will be based within our clinical trials unit at Icon Cancer Centre South Brisbane. Within the role you'll have the opportunity to work on innovative oncology and haematology clinical trials that are helping shape the future of cancer care.
As part of a highly experienced and supportive clinical trials team, you'll coordinate a diverse portfolio of studies in our fast‑paced research unit. This role will see you working alongside leading investigators, research nurses and clinical trial professionals.
This is an opportunity to contribute to research that gives patients access to tomorrow's treatments today while building a rewarding career in one of Australia's largest clinical trial networks.
Whether you're an experienced Clinical Research Coordinator looking for your next challenge, or an oncology professional interested in transitioning into research, we'd love to hear from you.
Why Join us?
Work on studies that matter
Be part of a team delivering cutting‑edge oncology and haematology research that has a direct impact on patient outcomes.
Gain exposure to early phase clinical trials
Develop your experience working on complex and innovative studies within an established Phase 1 Oncology Unit.
Build your career
Access structured training, ongoing professional development and opportunities to progress within a growing national research network.

Join a collaborative team
Work alongside experienced investigators, research nurses and clinical trial professionals who are passionate about delivering high‑quality research.

Enjoy a better work-life balance
Monday to Friday role with no weekends, allowing you to continue making a difference while maintaining balance outside of work

About the Role
As a Clinical Research Coordinator, you will play an important role in the successful delivery of oncology and haematology clinical trials from start‑up through to study close‑out.

You will work closely with participants, investigators, sponsors, and multidisciplinary teams to ensure studies are conducted safely, ethically and in accordance with protocol and regulatory requirements.

Key responsibilities include:

• Coordinating the day‑to‑day running of clinical trials
• Support participant recruitment and guide participants throughout their trial journey
• Work closely with investigators, sponsors, monitors and other stakeholders
• Coordinate study visits, assessments and trial related procedures
• Maintain study documentation and regulatory records
• Manage trial data collection and resolve data queries
• Assist with study start‑up activities to ensure site activation
• Ensure studies are conducted in line with the protocol, GCP and regulatory requirements

https://www.youtube.com/watch?v=YrHXzasueWw

Join a team at the forefront of cancer research
Due to ongoing expansion of our clinical trials program, we are seeking interested clinical trial professionals to join our team.
This permanent full-time role will be based within our clinical trials unit at Icon Cancer Centre South Brisbane. Within the role you'll have the opportunity to work on innovative oncology and haematology clinical trials that are helping shape the future of cancer care.
As part of a highly experienced and supportive clinical trials team, you'll coordinate a diverse portfolio of studies in our fast‑paced research unit. This role will see you working alongside leading investigators, research nurses and clinical trial professionals.
This is an opportunity to contribute to research that gives patients access to tomorrow's treatments today while building a rewarding career in one of Australia's largest clinical trial networks.
Whether you're an experienced Clinical Research Coordinator looking for your next challenge, or an oncology professional interested in transitioning into research, we'd love to hear from you.
Why Join us?
Work on studies that matter
Be part of a team delivering cutting‑edge oncology and haematology research that has a direct impact on patient outcomes.
Gain exposure to early phase clinical trials
Develop your experience working on complex and innovative studies within an established Phase 1 Oncology Unit.
Build your career
Access structured training, ongoing professional development and opportunities to progress within a growing national research network.

Join a collaborative team
Work alongside experienced investigators, research nurses and clinical trial professionals who are passionate about delivering high‑quality research.

Enjoy a better work-life balance
Monday to Friday role with no weekends, allowing you to continue making a difference while maintaining balance outside of work

About the Role
As a Clinical Research Coordinator, you will play an important role in the successful delivery of oncology and haematology clinical trials from start‑up through to study close‑out.

You will work closely with participants, investigators, sponsors, and multidisciplinary teams to ensure studies are conducted safely, ethically and in accordance with protocol and regulatory requirements.

Key responsibilities include:

• Coordinating the day‑to‑day running of clinical trials
• Support participant recruitment and guide participants throughout their trial journey
• Work closely with investigators, sponsors, monitors and other stakeholders
• Coordinate study visits, assessments and trial related procedures
• Maintain study documentation and regulatory records
• Manage trial data collection and resolve data queries
• Assist with study start‑up activities to ensure site activation
• Ensure studies are conducted in line with the protocol, GCP and regulatory requirements

About You
We're keen to hear from applicants who bring:

• Experience coordinating clinical research studies, or
• Oncology, haematology or broader healthcare experience with an interest in clinical research
• Strong organisational and time management skills
• Excellent communication and stakeholder management abilities
• High attention to detail and a commitment to quality
• The ability to work both independently and collaboratively within a multidisciplinary team

Experience in oncology, haematology or clinical trials is highly regarded but not essential for the right candidate.

What Success Looks Like
In your first 12 months, you'll:

• Build confidence managing a portfolio of clinical trials
• Develop expertise in oncology and haematology research
• Strengthen relationships with investigators, sponsors and research participants
• Contribute to successful study recruitment and delivery
• Become a valued member of a high‑performing research team helping advance cancer care

About Icon Research
Icon Research delivers world‑class clinical trials across a growing network of sites throughout Australia and internationally. Our teams are united by a shared commitment to improving patient outcomes through innovation, collaboration and excellence in research.

Every trial represents an opportunity to bring new treatment options to patients and contribute to the future of cancer care.