đ Launch Your Clinical Research Career in China
Join ICON plc, a global leader in healthcare intelligence, as a Clinical Research Associate I in China. This is your gateway to an exciting career in clinical research, where you'll gain hands-on experience managing clinical trial sites and contribute to the development of life-changing medical treatments. Perfect for motivated professionals ready to begin their journey in the dynamic Chinese clinical research market.
đ Your Impact: Key Responsibilities
Site Management & Coordination
- Coordinate all site activities from study setup through close-out
- Conduct site visits (qualification, initiation, monitoring, close-out)
- Maintain accurate study documentation and status reports
- Ensure proper clinical trial material management at sites
Compliance & Quality Assurance
- Ensure adherence to ICH-GCP guidelines and local regulations
- Verify patient safety and protocol compliance
- Review and evaluate clinical data for accuracy and completeness
- Support audit and inspection readiness activities
Stakeholder Engagement
- Build collaborative relationships with clinical investigators and site staff
- Serve as primary ICON representative at assigned sites
- Facilitate effective communication between sites and study team
- Address site queries and resolve issues proactively
Study Documentation & Efficiency
- Process sponsor-generated queries efficiently
- Participate in study documentation preparation and review
- Contribute to feasibility assessments for new proposals
- Support study cost-efficiency initiatives
â Your Profile: Qualifications & Experience
Essential Requirements
- University degree in Medicine, Life Sciences, or related field
- Understanding of ICH-GCP guidelines and clinical research principles
- Fluency in English and Mandarin (written and verbal)
- Willingness to travel up to 60% of the time
- Valid driver's license
Ideal Candidate Profile
- Strong interest in clinical research and patient care
- Excellent communication and interpersonal skills
- Proactive problem-solving abilities
- High attention to detail and organizational skills
- Ability to work effectively in a team environment
Preferred Attributes
- Previous exposure to clinical research environment
- Basic understanding of Chinese regulatory landscape
- Adaptability to fast-paced, dynamic work settings
đŤ Why Join ICON in China?
Career Launchpad
- Comprehensive CRA training and development program
- Clear career progression path to CRA II and beyond
- Mentorship from experienced clinical research professionals
- Exposure to diverse therapeutic areas and study phases
Professional Development
- Hands-on experience with global clinical trials
- Opportunities for continuous learning and certification
- Networking with industry experts and key opinion leaders
- Language and cultural proficiency development
Competitive Benefits
- Attractive entry-level salary package
- Comprehensive health insurance coverage
- Travel allowance and accommodation support
- Generous vacation entitlements
- Wellness programs and employee assistance
⨠Ready to Start Your CRA Journey in China?
If you're passionate about beginning a meaningful career in clinical research and meet our basic requirements, we encourage you to apply. We value potential and dedication - don't hesitate to submit your application even if you're new to the field!
Apply Now & Begin Your Clinical Research Adventure
