Clinical Trial Associate: Drive Global Trials & Data

ICON; Kuala Lumpur; On-site; MYR 60,000 - 90,000; Full time

Benefits offered by this job

Competitive benefits

Job summary

ICON Strategic Solutions is actively seeking a Clinical Trial Associate in Malaysia. You will assist in designing, analyzing, and interpreting trial data while supporting the advancement of new treatments. The role emphasizes collaboration with teams to ensure high-quality research outputs.

You will coordinate trials, maintain regulatory documentation, and help prepare essential study materials. Travel up to 10% is expected as part of the role within a global sponsor framework.

Qualifications

• 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 approximately 10%.

Responsibilities

• 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.

Skills

Organizational skills

Communication

Team collaboration

Attention to detail

Ability to travel

Education

Bachelor's degree in science/healthcare

Job description

ICON Strategic Solutions is actively seeking a Clinical Trial Associate in Malaysia. You will assist in designing, analyzing, and interpreting trial data while supporting the advancement of new treatments. The role emphasizes collaboration with teams to ensure high-quality research outputs.

You will coordinate trials, maintain regulatory documentation, and help prepare essential study materials. Travel up to 10% is expected as part of the role within a global sponsor framework.