Clinical Trial Coordinator

Cancer Care Foundation; Wollongong City Council; Sur place; AUD 70 000 - 90 000; Plein temps

Avantages offerts par ce poste

Salary packaging for tax-free income

Supportive work environment

Résumé du poste

Cancer Care Foundation (CCF) is seeking a Clinical Trial Coordinator at our Wollongong centre to manage oncology clinical trials. You will work closely with healthcare professionals to ensure trials are executed per protocols and GCP standards.

The ideal candidate has experience in clinical trials, strong communication skills, and the ability to work in a multidisciplinary environment. The role offers a supportive workplace where ideas are valued and includes salary packaging for tax-free income.

Qualifications

• At least 1 year of experience in a clinical trials environment.
• Solid understanding of clinical research and GCP.
• Ability to adapt to changing work conditions and meet deadlines.

Responsabilités

• Ensure clinical trials are executed according to protocols.
• Collaborate with a multidisciplinary team.
• Prepare and submit trial documentation.

Connaissances

Interpersonal skills

Communication skills

Planning and organization

Time management

Problem-solving

Clinical assessment

Computer skills

Formation

Tertiary qualification in medical or life sciences

Outils

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Electronic case report forms

Description du poste

Cancer Care Foundation (CCF) was established in 2018 as a not-for-profit charity organization dedicated to one clear purpose -creating the much-needed practical support for cancer patients to ease and improve their treatment journey so their energies are focused on getting well.

CCF manages clinical trials at multiple centres across Australia, with our Head Office located in Miranda NSW. Due to the growth of our clinical trials business, CCF requires a Clinical Trial Coordinator at our Wollongong centre who will play a key role in oncology clinical trials. You will be responsible for ensuring that clinical trials are executed in strict accordance with study-specific protocols, GCP standards, and organizational guidelines. You will work closely with a diverse team of doctors, nurses, clinical project managers, pharmacists, clinical trial coordinators, data managers, sponsor teams, and clinical research associates.

About You

To succeed in this role, you should meet the following criteria:

Australian work rights are required for this position, as is a Police Check .

A minimum of 1 year experience working in a clinical trials environment, ideally as a Clinical Trial Coordinator, with a solid understanding of clinical research and GCP.

Strong interpersonal and communication skills, with the ability to collaborate effectively with a broad range of stakeholders within a multidisciplinary environment.

Excellent planning, organisational, and time management skills, with a professional, reliable, and punctual approach to work.

Ability to adapt to changing work conditions and business needs to meet project deadlines, both autonomously and supporting colleagues.

A high level of ownership and accountability for clinical trial execution, with the initiative to resolve issues and find solutions.

Familiarity with ethics and governance processes and competence in preparing and submitting trial documentation is an advantage.

Experience with clinical assessment techniques (e.g., vital signs, ECG, venipuncture) and laboratory procedures (e.g., blood and urine processing, centrifugation, pipetting) is strongly preferred. Note, training is provided.

Strong computer skills, including experience with electronic case report forms, Microsoft Word, Excel, and PowerPoint, is an advantage.

A tertiary qualification in medical, life sciences, nursing, or a related field is preferred, but not mandatory.

Some travel is preferred but not mandatory.

Advantages of working at CCF:

Salary packaging allowing up to $15,000 tax free income.

Supportive work environment where your ideas are valued and encouraged.