Clinical Trial Associate: Accelerate Medical Innovation

ICON Docs division Malaysia; Kuala Lumpur; On-site; MYR 60,000 - 80,000; Full time

Job summary

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. This role places you at the core of trial design, data interpretation and collaboration with cross-functional teams to deliver high-quality clinical research work.

You will coordinate trials, maintain essential documents, support informed consent and case report forms, and help track milestones and regulatory submissions.

Qualifications

• Bachelor's degree in a scientific or healthcare field.
• Experience or strong interest in clinical research.
• Knowledge of clinical trial processes, regulations, and guidelines.
• Excellent organizational and communication skills.

Responsibilities

• Assist in coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
• Maintain and organize 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

Clinical research

Regulatory knowledge

Organizational skills

Communication skills

Travel readiness

Education

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

Job description

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. This role places you at the core of trial design, data interpretation and collaboration with cross-functional teams to deliver high-quality clinical research work.

You will coordinate trials, maintain essential documents, support informed consent and case report forms, and help track milestones and regulatory submissions.