đŹ Advance Clinical Research in China's Capital
Join ICON plc in Beijing as a Clinical Research Associate II and take your clinical research career to the next level. This hybrid role offers the perfect balance of field monitoring and office-based collaboration, allowing you to manage complex clinical trial sites while contributing to groundbreaking medical advancements in one of the world's most dynamic healthcare markets.
đŻ Your Impact: Key Responsibilities
Site Management Excellence
- Conduct comprehensive site visits (qualification, initiation, monitoring, close-out)
- Ensure protocol compliance and maintain highest standards of data integrity
- Serve as primary point of contact for assigned clinical sites in Beijing region
- Perform source data verification and query resolution
Quality & Compliance Leadership
- Ensure adherence to ICH-GCP guidelines and Chinese regulatory requirements
- Maintain sites in audit and inspection-ready state
- Review and manage essential study documentation
- Monitor patient safety and protocol compliance
Stakeholder Collaboration
- Build strong relationships with investigators and site staff
- Collaborate with cross-functional study teams
- Provide expert guidance on site management best practices
- Contribute to study documentation and clinical study reports
Study Execution
- Develop site-specific patient recruitment strategies
- Manage investigational product accountability
- Ensure timely data entry and query resolution
- Support site training and capability development
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
- Experience with Chinese regulatory environment and site requirements
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 Beijing?
Career Progression
- Clear pathway to Senior CRA and leadership roles
- Hybrid working model offering flexibility
- Exposure to global clinical trials and innovative therapies
- Professional development and training programs
Strategic Location
- Work in China's capital with access to leading medical institutions
- Balance field monitoring with office-based collaboration
- Network with key opinion leaders in Chinese healthcare
- Experience in one of the world's fastest-growing clinical research markets
Comprehensive Benefits
- Competitive compensation package
- Flexible hybrid working arrangements
- Comprehensive health insurance for you and family
- Retirement planning and financial security programs
- Generous vacation entitlements and wellness support
⨠Ready to Elevate Your Career in Beijing?
If you're an experienced CRA looking to advance your career in a dynamic market with flexible working options, we encourage you to apply. Join us in shaping the future of clinical development in China.
Apply Now & Make Your Mark in Clinical Research
