Senior Clinical Trial Operations Specialist

ICON Docs division Malaysia; Kuala Lumpur; On-site; MYR 90,000 - 150,000; Full time

Benefits offered by this job

Competitive base salary

Health and wellbeing programme

Retirement and pension plans

Life assurance

Employee assistance programmes

Learning and development opportunities

Job summary

ICON Plc, a global healthcare intelligence and clinical research organisation, seeks a Senior Clinical Trial Associate in Kuala Lumpur. You will manage trial deliverables, support regulatory submissions, and coordinate with cross-functional teams to ensure study success.

You will operate independently, guiding others, with a focus on documentation, compliance, and timely communication across sites. A strong background in trial support and meticulous data management is essential.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Extensive experience in a clinical trial support role with knowledge of trial processes and regulations.
• Strong organizational and multitasking skills with attention to detail.

Responsibilities

• Provide administrative support for clinical trials, including documentation management and trial records.
• Assist in preparation and submission of regulatory documents and ensure protocol compliance.
• Collaborate with cross-functional teams to support trial operations and resolve issues.

Education

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

Extensive experience in a clinical trial support role

Tools

CTMS (clinical trial management system)

Regulatory documentation tools

Job description

ICON Plc, a global healthcare intelligence and clinical research organisation, seeks a Senior Clinical Trial Associate in Kuala Lumpur. You will manage trial deliverables, support regulatory submissions, and coordinate with cross-functional teams to ensure study success.

You will operate independently, guiding others, with a focus on documentation, compliance, and timely communication across sites. A strong background in trial support and meticulous data management is essential.