đŹ Advance Clinical Research in Malaysia
Join ICON plc as a Clinical Research Associate II in Malaysia and take your career to the next level in clinical research. This office-based role with extensive travel offers the opportunity to manage clinical trial sites across Malaysia, ensuring the highest standards of research quality while contributing to the development of innovative medical treatments that improve patient lives.
đŻ Your Impact: Key Responsibilities
Site Management & Monitoring
- Conduct comprehensive site visits (qualification, initiation, monitoring, close-out) across Malaysia
- Serve as primary point of contact for assigned clinical trial sites
- Perform source data verification and ensure data integrity
- Develop and implement site-specific patient recruitment strategies
Quality & Compliance Excellence
- Ensure adherence to ICH-GCP guidelines and Malaysian regulatory requirements
- Maintain sites in audit and inspection-ready state
- Monitor patient safety and protocol compliance
- Review and manage essential study documentation
Stakeholder Collaboration
- Build strong relationships with investigators and site staff
- Collaborate with cross-functional study teams
- Facilitate effective communication between sites and study management
- Provide expert guidance on site management best practices
Study Documentation & Execution
- Contribute to study documentation and clinical study reports
- Manage investigational product accountability
- Ensure timely data entry and query resolution
- Support regulatory submission preparations
â Your Profile: Qualifications & Experience
Essential Requirements
- Bachelor's degree in Life Sciences, Medicine, or healthcare-related field
- Minimum 2 years of experience as a Clinical Research Associate
- Comprehensive knowledge of ICH-GCP guidelines and clinical trial processes
- Fluency in English and Bahasa Malaysia
- Willingness to travel up to 60% within Malaysia
- Valid driver's license
Technical Competencies
- Proficiency with Clinical Trial Management Systems (CTMS)
- Strong data management and documentation skills
- Experience with electronic data capture systems
- Monitoring visit report writing and documentation
Professional Attributes
- Excellent organizational and communication skills
- Strong problem-solving and decision-making abilities
- Ability to work independently and in team environments
- Cultural awareness and adaptability
- Attention to detail and quality focus
đŤ Why Join ICON in Malaysia?
Career Progression
- Clear pathway to Senior CRA and leadership roles
- Office-based with extensive field exposure
- Exposure to global clinical trials and innovative therapies
- Professional development and training programs
Strategic Location
- Work across Malaysia's leading medical institutions
- Balance office collaboration with field monitoring
- Network with key opinion leaders in Malaysian healthcare
- Experience in Southeast Asia's growing clinical research market
Comprehensive Benefits
- Competitive compensation package
- Comprehensive health insurance for you and family
- Retirement planning and financial security programs
- Generous vacation entitlements and wellness support
- Global employee assistance program
⨠Ready to Advance Your Career in Malaysia?
If you're an experienced CRA looking to grow your career in Malaysia's dynamic clinical research environment, we encourage you to apply. Join us in shaping the future of clinical development while enjoying the professional opportunities across Malaysia.
Apply Now & Make Your Mark in Malaysian Clinical Research
