Senior Clinical Trial Associate — Clinical Ops & Compliance

ICON Strategic Solutions (FSP); Kuala Lumpur; On-site; MYR 120,000 - 180,000; Full time

Job summary

ICON Strategic Solutions in Kuala Lumpur is seeking a Senior Clinical Trial Associate to support trial management and regulatory activities in a sponsor-dedicated model.

You will own trial deliverables, manage documentation, coordinate meetings, and ensure compliance with study protocols and regulatory requirements. The role requires strong organizational skills and willingness to travel up to 10%.

Qualifications

• Strong communication, interpersonal and problem-solving skills.
• Excellent organizational and multitasking abilities to manage multiple trials and tasks.
• Proficiency with clinical trial management systems and regulatory documentation tools.

Responsibilities

• Providing administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records.
• Assisting in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements.
• Collaborating with cross-functional teams to support trial operations and resolve any issues that arise during the course of the study.
• Monitoring and tracking trial progress, including managing site communications and ensuring timely delivery of study materials.
• Building and maintaining strong relationships with site staff and other stakeholders to facilitate smooth trial operations and support overall project success.

Skills

Communication

Interpersonal skills

Problem-solving

Organization & multitasking

Attention to detail

Travel willingness

Education

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

Tools

Clinical trial management systems

Regulatory documentation software

Job description

ICON Strategic Solutions in Kuala Lumpur is seeking a Senior Clinical Trial Associate to support trial management and regulatory activities in a sponsor-dedicated model.

You will own trial deliverables, manage documentation, coordinate meetings, and ensure compliance with study protocols and regulatory requirements. The role requires strong organizational skills and willingness to travel up to 10%.