Clinical Trial Coordinator, Medical Oncology

Clueo Clinical Pty Ltd; Liverpool; On-site; AUD 40,000 - 80,000; Full time

Job summary

An innovative organization is seeking a Clinical Trial Coordinator to enhance cancer research efforts. This role involves supporting Medical Oncologists in clinical trials, managing participant recruitment, and ensuring compliance with study protocols. The successful candidate will thrive in a collaborative environment, benefiting from a competitive salary and professional development opportunities. Join a team that values imagination, inclusion, and integrity, making a significant impact on health outcomes. If you have a passion for research and a commitment to excellence, this position offers a rewarding career path.

Benefits

Competitive Salary

Salary Packaging Opportunities

Meal Entertainment Card

Ongoing Training

Collaborative Team Culture

Close to Shopping Centres

Qualifications

• Minimum 3 years experience as a Clinical Trial Coordinator.
• Strong project planning and coordination skills required.

Responsibilities

• Support cancer clinical trials and assist with research activities.
• Evaluate and recruit eligible participants for clinical trials.

Skills

Project Planning

Coordination

Time Management

Communication Skills

Problem Solving

Interpersonal Skills

Computing Skills

Clinical Research Knowledge

Education

Degree in Health Science or Nursing

Tools

Clinical Trial Electronic Data Entry

Databases

Spreadsheets

Job description

Clinical Trial Coordinator, Medical Oncology

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At Ingham Institute for Applied Medical Research (“Ingham Institute"), we are committed to inspiring better health and transforming the treatment and care of people living with the most prevalent medical conditions and diseases. Our purpose is to make and apply discoveries that translate to radical improvement in health and health care for all.

We are a values-based, equal opportunity employer committed to equity, diversity, and inclusion. Our values act as a guide for our behaviours and engagement with our colleagues, partners, stakeholders, and the communities we support.

Our values

Imagination – we boldly challenge each other to think differently.

Inclusion – we believe in and direct our efforts towards equity for all.

Impact – we maximise our success by being relevant, focused, and responsive.

Integrity – we operate with honesty and transparency in everything we do.

About the role

Due to growth in the department, we are seeking an experienced Clinical Trials Coordinator to join our Medical Oncology Clinical Trial Unit, on a 12-month, Full-Time contract.

The Clinical Trial Coordinator will work with Medical Oncologists in support of cancer clinical trials and will assist with research activities of the Medical Oncology Department, including the evaluation and recruitment of eligible participants to clinical trials, research studies, implementing and monitoring study protocols and documentation associated with the studies/trials.

The complete position description is available upon request (please contact Hayley Paris at [emailprotected]).

Minimum experience and qualifications:

• A degree in health science or nursing.
• Highly developed project planning, coordination, organisation and time management skills.
• Proven ability to identify problems, make recommendations and implement appropriate solutions in the research environment.
• Strong communication and organisation skills.
• High level interpersonal skills and proven ability to work strategically with key stakeholders in a research environment.
• Well-developed written and verbal communication skills and consultation skills.
• High level computing skills, including databases, clinical trial electronic data entry, work processing and spreadsheets.
• Previous experience in sponsored clinical trials.
• Detailed knowledge of clinical research practices, ethical obligations, ICH and Good Clinical Practice.
• Ability and willingness to travel to attend conferences and investigator meetings.
• Demonstrated ability to maintain high work standards with minimum supervision and to ensure team compliance with Standard Operating Procedures relevant to clinical trial conduct.
• Flexibility in work hours (as required).

What we offer

At the Ingham Institute, we are proud to offer a dynamic and supportive work environment that fosters professional development and work-life balance. Key benefits include:

• A competitive salary plus access to salary packaging opportunities (up to $15,900 of general living expenses including rent, mortgage, and credit card payments each year).
• A Meal Entertainment card (salary packaging up to $2,650 for dining out, hotel accommodation, venue hire, and catering expenses annually).
• State-of-the-art research facilities and resources.
• Opportunities for ongoing training and career progression.
• A collaborative team culture.
• Office located close to major shopping centres and transport hubs.

Application process

All applications must be submitted via SEEK and include:

• A cover letter (maximum two pages) detailing your relevant experience as a Clinical Trials Coordinator, highlighting project planning, coordination, organisation, and time management skills.

Applicants must have existing Australian work rights. Offers of employment are contingent upon a satisfactory National Police Check, which assesses only information relevant to the job requirements. Salary packaging opportunities are available as the Institute is endorsed as a Deductible Gift Recipient.

Please note that only shortlisted applicants who include the correct application documents will be contacted.

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• How many years' experience do you have as a Clinical Trial Coordinator?
• Which statement best describes your right to work in Australia?
• How many years' experience do you have as a Research Coordinator?
• What is your expected annual base salary?
• How much notice are you required to give your current employer?
• Which statement best describes your Covid-19 vaccination status?

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