Senior Clinical Research Associate

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

Job summary

A leading healthcare intelligence organization based in Kuala Lumpur is seeking a Senior Clinical Research Associate. You will play a vital role in overseeing clinical trial activities, ensuring protocol adherence and data integrity. The ideal candidate should have an advanced degree in a relevant field and extensive experience in clinical trial processes. This position involves significant travel. Join us and contribute to shaping the future of clinical development.

Qualifications

• Extensive experience as a Clinical Research Associate with strong understanding of clinical trial processes.
• Proven ability to manage multiple sites and projects simultaneously.
• Excellent communication and stakeholder management skills.

Responsibilities

• Monitoring clinical trial sites to ensure adherence to protocols and regulatory requirements.
• Conducting site visits to assess site performance and resolve issues.
• Providing training and guidance to site staff to maintain high standards.

Skills

Clinical trial management

Data integrity

Interpersonal skills

Stakeholder management

Problem-solving

Education

Advanced degree in life sciences, nursing, or medicine

Tools

Clinical trial software

Job description

Overview

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

Responsibilities

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
• Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile

• Advanced degree in a relevant field such as life sciences, nursing, or medicine.
• Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
• Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
• Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
• Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.

Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

What ICON can offer you

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

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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

Note

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