đŹ Advance Clinical Research in Shanghai with Flexible Working
Join ICON plc in Shanghai as a Clinical Research Associate II and elevate your career in one of Asia's most dynamic healthcare markets. This hybrid role offers the perfect balance of site monitoring and office-based collaboration, allowing you to manage clinical trial sites while enjoying flexible working arrangements in China's commercial capital.
đŻ Your Impact: Key Responsibilities
Site Management Excellence
- Conduct comprehensive site visits (qualification, initiation, monitoring, close-out)
- Serve as primary point of contact for assigned clinical sites in Shanghai region
- Perform source data verification and ensure data integrity
- Develop site-specific patient recruitment strategies
Quality & Compliance Leadership
- Ensure adherence to ICH-GCP guidelines and Chinese 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 Mandarin (written and verbal)
- 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 Shanghai?
Career Progression
- Clear pathway to Senior CRA and leadership roles
- Hybrid working model offering office flexibility
- Exposure to global clinical trials and innovative therapies
- Professional development and training programs
Strategic Location
- Work in China's commercial capital with leading medical institutions
- Balance field monitoring with office-based collaboration
- Network with key opinion leaders in Chinese healthcare
- Experience in Asia's fastest-growing clinical research market
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 Advance Your Career in Shanghai?
If you're an experienced CRA looking to grow 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 while enjoying the best of Shanghai's professional opportunities.
Apply Now & Make Your Mark in Clinical Research
