đĽ Advance Clinical Research in China's Capital
Join ICON plc as a Clinical Research Associate II in Beijing and take your clinical research career to the next level. This office-based role with extensive travel offers the opportunity to manage clinical trial sites across China while contributing to groundbreaking medical research from our strategic Beijing location.
đŻ Your Impact: Key Responsibilities
Site Management & Monitoring Excellence
- Conduct comprehensive site qualification, initiation, monitoring, and close-out visits
- Serve as primary point of contact for assigned clinical sites in the Beijing region
- Perform source data verification and ensure data integrity across all sites
- Develop and implement effective patient recruitment strategies
Quality & Regulatory Compliance
- Ensure strict adherence to ICH-GCP guidelines and Chinese regulatory requirements
- Maintain all sites in audit-ready condition
- Monitor patient safety and protocol compliance throughout trial duration
- Review and manage essential study documentation to regulatory standards
Stakeholder Collaboration & Leadership
- Build and maintain strong relationships with investigators and site staff
- Collaborate effectively with cross-functional study teams
- Provide expert guidance on site management best practices
- Facilitate clear communication between sites and study management
Study Documentation & Execution
- Contribute to preparation of clinical study reports and protocols
- Manage investigational product accountability and documentation
- Ensure timely data entry and query resolution
- Support regulatory submission preparations as required
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 Mandarin (written and verbal)
- Willingness to travel up to 60% (domestic within China)
- Valid driver's license
Technical Competencies
- Proficiency with Clinical Trial Management Systems (CTMS)
- Strong experience with electronic data capture systems
- Excellent monitoring visit report writing skills
- Understanding of Chinese regulatory landscape
Professional Attributes
- Exceptional organizational and communication skills
- Strong problem-solving and decision-making capabilities
- Ability to work independently and in collaborative team environments
- High attention to detail and quality-focused approach
- Cultural awareness and adaptability
đŤ Why Join ICON in Beijing?
Career Advancement Opportunities
- Clear pathway to Senior CRA and leadership positions
- Office-based role with comprehensive field exposure
- Professional development and specialized training programs
- Exposure to global clinical trials across multiple therapeutic areas
Strategic Beijing Location
- Work from China's capital with access to leading medical institutions
- Balance office collaboration with extensive site monitoring
- Network with key opinion leaders in Chinese healthcare
- Experience in Asia's fastest-growing clinical research market
Comprehensive Benefits Package
- Competitive compensation with performance incentives
- Comprehensive health insurance for you and your family
- Retirement planning and financial security programs
- Generous vacation entitlements and wellness support
- Global employee assistance program
⨠Ready to Advance Your Career in Beijing?
If you're an experienced CRA looking to grow your career in China's dynamic clinical research environment, we encourage you to apply. Join us in shaping the future of clinical development while advancing your professional journey from our Beijing office.
Apply Now & Make Your Mark in Chinese Clinical Research
