Clinical Trial Assistant

ICON Clinical Research; Sydney; On-site; AUD 70,000 - 90,000; Full time

Benefits offered by this job

Competitive base salary

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes and wel

Learning and development opportunities

Job summary

ICON Strategic Solutions is seeking a Clinical Trial Associate in Sydney with a focus on delivering high-quality clinical research work. You will assist with design and analysis of trials, interpreting complex medical data, and contribute to transformative therapies.

In this sponsor-dedicated role, you will coordinate trials, maintain documentation, and prepare materials such as informed consent forms. Strong organizational and communication skills are essential, with travel approximately 10% as

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Experience or strong interest in clinical research.
• Knowledge of trial processes, regulations, and guidelines.
• Excellent organizational and communication skills.
• Ability to work collaboratively in a fast-paced environment.
• Willingness to travel approximately 10%.

Responsibilities

• Coordinate and administer clinical trials in compliance with protocols.
• Maintain study files, essential documents, and regulatory submissions.
• Prepare study materials like informed consent and case report forms.
• Collaborate with cross-functional teams to ensure smooth trial execution.
• Track and report clinical trial metrics and milestones.

Education

Bachelor's degree in a scientific or healthcare-related field

Job description

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

• Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
• Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
• Support the preparation of study-related materials, such as informed consent forms and case report forms.
• Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
• Contribute to the tracking and reporting of clinical trial metrics and milestones.

Your Profile:

You will bring relevant clinical research experience, along with the following qualifications and skills.

Required qualifications and experience:

• Bachelor's degree in a scientific or healthcare-related field.
• Prior experience or strong interest in clinical research.
• Knowledge of clinical trial processes, regulations, and guidelines.
• Excellent organizational and communication skills.
• Ability to work collaboratively in a fast-paced environment with attention to detail.
• Willingness to travel as required (approximately 10%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.