Clinical Trials Associate — Study Coordination & Data Insight

ICON Strategic Solutions (FSP); Sydney; On-site; AUD 60,000 - 90,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement plans

EAP LifeWorks

Life insurance

Flexible benefits

Job summary

ICON Strategic Solutions (FSP) in Sydney NSW is seeking a Clinical Trial Associate to support design and analysis of clinical trials, interpret medical data, and contribute to the development of innovative treatments.

You will coordinate trials, maintain study documentation, prepare materials like informed consent forms, and collaborate with cross-functional teams to ensure timely trial execution and milestone tracking.

Qualifications

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

Responsibilities

• Coordinate and administer clinical trials, ensuring compliance with protocols and regulatory requirements.
• Maintain and organize clinical trial documentation, including study files and regulatory submissions.
• Assist in preparing study-related materials, such as informed consent forms and case report forms.
• Collaborate with cross-functional teams to facilitate communication and trial execution.
• Track and report clinical trial metrics and milestones.

Skills

Clinical research experience

Organizational skills

Communication skills

Team collaboration

Attention to detail

Travel readiness

Education

Bachelor's degree in a scientific field

Job description

ICON Strategic Solutions (FSP) in Sydney NSW is seeking a Clinical Trial Associate to support design and analysis of clinical trials, interpret medical data, and contribute to the development of innovative treatments.

You will coordinate trials, maintain study documentation, prepare materials like informed consent forms, and collaborate with cross-functional teams to ensure timely trial execution and milestone tracking.