Clinical Trial Operations Specialist

ICON; Singapore; On-site; SGD 50,000 - 80,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme (

Life assurance

Job summary

ICON Strategic Solutions is seeking a Clinical Trial Administrator in Singapore to support the design and analysis of clinical trials and ensure regulatory compliance. You will coordinate trial activities, maintain essential documents, and work with cross-functional teams to drive study milestones.

The role requires a scientific or healthcare background, interest in clinical research, and strong organizational/communication skills to manage fast-paced environments and regulatory demands.

Qualifications

• Bachelor's degree in a scientific or healthcare field.
• Experience or strong interest in clinical research; CTRAs preferred.
• Knowledge of clinical trial processes, regulations, and guidelines; experience in trial supplies preferred.
• Excellent organizational and communication skills.
• Ability to work collaboratively in a fast-paced environment with attention to detail.

Responsibilities

• Assist in coordinating and administering clinical trials, ensuring protocol compliance.
• Maintain and organize trial documentation and regulatory submissions.
• Prepare study materials such as informed consent forms and CRFs.
• Collaborate with cross-functional teams to ensure smooth trial execution.
• Track and report clinical trial metrics and milestones.

Skills

Organizational skills

Communication skills

Attention to detail

Collaboration

Regulatory knowledge

Education

Bachelor's degree in science/healthcare

Job description

ICON Strategic Solutions is seeking a Clinical Trial Administrator in Singapore to support the design and analysis of clinical trials and ensure regulatory compliance. You will coordinate trial activities, maintain essential documents, and work with cross-functional teams to drive study milestones.

The role requires a scientific or healthcare background, interest in clinical research, and strong organizational/communication skills to manage fast-paced environments and regulatory demands.