ICON

Senior Clinical Trial Associate

Malaysia · Work style not stated · Full time

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About the role

Description from the employer’s posting. Check the employer’s page for the current version.

EmployerICON
LocationMalaysia
Work styleWork style not stated
Employment typeFull time
Employer posted2 Oct 2026

Senior CTA

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Senior Clinical Trial Associate at ICON Plc, you will support the management and execution of clinical trials by handling a range of administrative and operational tasks.

What You Will Do:

You will take ownership of clinical trial management deliverables, applying your expertise to complex challenges.

Key responsibilities include:

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.

Show full description

Your Profile:

You will have a strong foundation in clinical trial management, with the experience to work independently and guide others.

Required qualifications and experience:

Bachelor's degree in a relevant scientific discipline or healthcare-related field
Extensive experience in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements.
Strong organizational and multitasking skills, with the ability to manage multiple tasks and projects effectively.
Proficiency in clinical trial management systems and relevant software, with a keen eye for detail in documentation and data management.
Excellent communication, interpersonal, and problem-solving skills, with the ability to work collaboratively with diverse teams and stakeholders.
Willingness to travel as required (approximately 10%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

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