Clinical Trial Associate - Global Team, Impactful Research

ICON Clinical Research; Sydney; Sur place; AUD 70 000 - 90 000; Plein temps

Avantages offerts par ce poste

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

Résumé du poste

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%.

Responsabilités

• 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.

Formation

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

Description du poste

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