Clinical Trials Coordinator at Ramsay Health Care Australia

virginia, Virginia, Australia -

Full Time

Start Date

Immediate

Expiry Date

27 Dec, 26

Salary

4000.0

Posted On

28 Sep, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Yes

Skills

Industry

Hospitals & Health Systems

Description

About the job

Company Description

Through seed funding provided by the Ramsay Hospital Research Foundation, Ramsay Health Care has established a national clinical trials network. Consisting of 22 sites spread across four states of Australia, the network employs over 60 team members who focus on the establishment and development of clinical trials at our sites. Our clinical trial activities focus on Oncology & Haematology, Mental Health, Musculoskeletal Disease and Cardiology as well as other therapeutic areas such as respiratory and neurology. Through this dedicated network Ramsay Health Care is able to provide access to emerging treatments and new devices that offer a participant the potential of changing the outcomes of any diagnosis and disease.

The role will report to the Clinical Trials Unit and Research Manager and will work closely with a number of key stakeholders including the clinical trials team, the Hospital finance teams and the National Clinical Trials Network.

Job Description

About The Role

Join our team as a Clinical Trials Coordinator on a full-time permanent basis!

The Clinical Trials Coordinator is responsible for the day-to-day coordination and management of clinical research studies conducted at Ramsay Clinic Northside, ensuring compliance with Good Clinical Practice (GCP), study protocols, ethical requirements, and regulatory standards. The role supports the delivery of high-quality mental health research by coordinating participant recruitment, assessments, data collection, and study administration while maintaining participant safety and wellbeing.

Key Responsibilities

Coordinate all aspects of clinical trials from study start-up through to close-out.
Screen, recruit, consent, and retain study participants in accordance with approved protocols.
Conduct study visits, assessments, and data collection activities as delegated by the Principal Investigator.
Maintain accurate and timely study documentation, source records, and case report forms.
Ensure compliance with Human Research Ethics Committee (HREC), Therapeutic Goods Administration (TGA), ICH-GCP, and sponsor requirements.
Liaise with investigators, sponsors, contract research organisations (CROs), pharmacists, and other healthcare professionals.
Coordinate study monitoring visits, audits, and regulatory submissions.
Manage participant scheduling and follow-up appointments.
Monitor adverse events and report safety information according to study and regulatory requirements.
Maintain research databases and ensure data quality, confidentiality, and integrity.
Assist with study feasibility assessments, site initiation activities, and participant recruitment strategies.
Support continuous improvement initiatives and contribute to the growth of the clinic's research program.

About You

To be successful in this role, you will bring:

Experience coordinating clinical trials and/or conducting clinical research.
Relevant qualification in Nursing, Psychology, Health Sciences, or a related field.
Knowledge of ICH-GCP guidelines, ethics processes, and clinical trial regulations.
Strong organisational, time-management, and multitasking skills.
Excellent communication and interpersonal skills, with the ability to engage sensitively with participants experiencing mental health conditions.
High level of attention to detail and accuracy in documentation.
Ability to work independently while collaborating effectively with multidisciplinary teams.
Proficiency in Microsoft Office, clinical trials management systems and clinical research databases.

Key Attributes

Patient-centred and compassionate approach.
Strong commitment to research quality and participant safety.
Ability to manage competing priorities in a fast-paced environment.
Professional, ethical, and accountable in all aspects of research conduct.

What’s In It For You:

At Ramsay, we care for our people by offering benefits that truly support your career, wellbeing and lifestyle, including:

Grow your career with recognition programs, employee referral bonuses, scholarships, free access to LinkedIn Learning and the Ramsay Leadership Academy
Save more every day with Ramsay Rewards, giving you exclusive deals at 100+ retailers, restaurants, travel providers and more
Enjoy peace of mind with lower hospital cover costs and higher extras limits on services like General and Major Dental, plus pharmacy and allied health discounts
Find balance through flexible rostering options, flexible leave and access to free, confidential counselling and wellbeing support 24/7
Increase your take-home pay through salary packaging and novated leasing, plus discounts on leisure travel, gyms and lifestyle services.

Why Join Ramsay:

At Ramsay Health Care, “people caring for people” is at the heart of everything we do. We are:

Australia’s largest private hospital operator, with over 74 sites and 35,000 staff
A values-led workplace where you’ll be supported personally and professionally
A place with flexible, permanent and career-growth opportunities nationwide.

Additional Information

Must provide or complete a National Police Check conducted within the previous 12 months.
According to the role, Ramsay may require a Working-With-Children Check and proof of immunisation against infectious diseases.

Apply:

All applications must be lodged online.

Applications close: 20th October 2026

Reference number: JR115669

Additional Information

Please Note:

Ramsay Health Care is committed to Child Safety. Details of our commitment are set out in our Code of Conduct, available at www.ramsayhealth.com.au.

Applications made by recruitment agencies will not be considered.

Responsibilities

About the job

Company Description

Job Description

About The Role

Join our team as a Clinical Trials Coordinator on a full-time permanent basis!

Key Responsibilities

Coordinate all aspects of clinical trials from study start-up through to close-out.
Screen, recruit, consent, and retain study participants in accordance with approved protocols.
Conduct study visits, assessments, and data collection activities as delegated by the Principal Investigator.
Maintain accurate and timely study documentation, source records, and case report forms.
Ensure compliance with Human Research Ethics Committee (HREC), Therapeutic Goods Administration (TGA), ICH-GCP, and sponsor requirements.
Liaise with investigators, sponsors, contract research organisations (CROs), pharmacists, and other healthcare professionals.
Coordinate study monitoring visits, audits, and regulatory submissions.
Manage participant scheduling and follow-up appointments.
Monitor adverse events and report safety information according to study and regulatory requirements.
Maintain research databases and ensure data quality, confidentiality, and integrity.
Assist with study feasibility assessments, site initiation activities, and participant recruitment strategies.
Support continuous improvement initiatives and contribute to the growth of the clinic's research program.

About You

To be successful in this role, you will bring:

Experience coordinating clinical trials and/or conducting clinical research.
Relevant qualification in Nursing, Psychology, Health Sciences, or a related field.
Knowledge of ICH-GCP guidelines, ethics processes, and clinical trial regulations.
Strong organisational, time-management, and multitasking skills.
Excellent communication and interpersonal skills, with the ability to engage sensitively with participants experiencing mental health conditions.
High level of attention to detail and accuracy in documentation.
Ability to work independently while collaborating effectively with multidisciplinary teams.
Proficiency in Microsoft Office, clinical trials management systems and clinical research databases.

Key Attributes

Patient-centred and compassionate approach.
Strong commitment to research quality and participant safety.
Ability to manage competing priorities in a fast-paced environment.
Professional, ethical, and accountable in all aspects of research conduct.

What’s In It For You:

At Ramsay, we care for our people by offering benefits that truly support your career, wellbeing and lifestyle, including:

Grow your career with recognition programs, employee referral bonuses, scholarships, free access to LinkedIn Learning and the Ramsay Leadership Academy
Save more every day with Ramsay Rewards, giving you exclusive deals at 100+ retailers, restaurants, travel providers and more
Enjoy peace of mind with lower hospital cover costs and higher extras limits on services like General and Major Dental, plus pharmacy and allied health discounts
Find balance through flexible rostering options, flexible leave and access to free, confidential counselling and wellbeing support 24/7
Increase your take-home pay through salary packaging and novated leasing, plus discounts on leisure travel, gyms and lifestyle services.

Why Join Ramsay:

At Ramsay Health Care, “people caring for people” is at the heart of everything we do. We are:

Australia’s largest private hospital operator, with over 74 sites and 35,000 staff
A values-led workplace where you’ll be supported personally and professionally
A place with flexible, permanent and career-growth opportunities nationwide.

Additional Information

Must provide or complete a National Police Check conducted within the previous 12 months.
According to the role, Ramsay may require a Working-With-Children Check and proof of immunisation against infectious diseases.

Apply:

All applications must be lodged online.

Applications close: 20th October 2026

Reference number: JR115669

Additional Information

Please Note:

Ramsay Health Care is committed to Child Safety. Details of our commitment are set out in our Code of Conduct, available at www.ramsayhealth.com.au.