Remote Job at ICON
Experienced professionals seeking Clinical research jobs and high-impact Remote Jobs will find this role especially compelling. This Senior Clinical Research Associate opportunity with ICON plc offers global exposure, leadership in clinical monitoring, and flexibility within Jobs in Kuala Lumpur, making it an excellent jobs opportunity for life science graduates progressing into senior clinical roles.
About the Company
ICON plc is a globally recognized leader in clinical research and healthcare intelligence. Through ICON plc Careers, professionals contribute to groundbreaking clinical trials across multiple therapeutic areas. ICON supports innovation, diversity, and flexible working models, including Remote Jobs, making it a preferred employer for experienced Clinical Research Associate professionals worldwide.
Remote Job Details
- Job Title: Senior Clinical Research Associate (Senior CRA)
- Location: Kuala Lumpur
- Job Reference ID: JR143310
- Business Unit: Clinical Monitoring – ICON Strategic Solutions
- Work Type: Remote
Role Overview
ICON is seeking an experienced Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. In this role, you will oversee and manage clinical trial activities to ensure compliance with study protocols, regulatory requirements, and industry standards. You will play a key role in maintaining data integrity, participant safety, and overall trial success throughout the study lifecycle.
Key Responsibilities
- Monitor clinical trial sites to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
- Conduct site visits to evaluate site performance, resolve issues, and support successful trial execution
- Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting
- Provide training and guidance to site staff and other CRAs to maintain high-quality clinical trial conduct
- Build and maintain strong relationships with site personnel and key stakeholders to support smooth trial operations
Candidate Profile
- Advanced degree in life sciences, or a related field
- Extensive experience as a Clinical Research Associate with strong knowledge of clinical trial processes and regulatory requirements
- Demonstrated ability to manage multiple sites and projects simultaneously
- Strong expertise in monitoring practices, data integrity, and site management
- Proficiency with clinical trial software and monitoring tools
- Excellent communication, interpersonal, and stakeholder management skills
- Ability to travel at least 60% (international and domestic; fly and drive)
- Valid driver’s license required
What ICON Offers in a Remote Job?
ICON’s success is built on the strength of its people. We prioritize a diverse, inclusive culture that rewards performance and supports personal and professional growth.
Benefits may include:
- Competitive salary
- Various annual leave entitlements
- Comprehensive health insurance options for you and your family
- Competitive retirement planning programs
- Global Employee Assistance Programme (LifeWorks) with 24/7 access to over 80,000 specialists worldwide
- Life assurance
- Flexible, country-specific benefits such as childcare vouchers, bike purchase schemes, gym discounts, subsidized travel passes, and health assessments
