📍 Launch Your Clinical Research Career as CRA I - China
Join ICON plc in China as a Clinical Research Associate I and embark on an exciting career journey in clinical development. This entry-level position offers comprehensive training and mentorship while you gain hands-on experience coordinating clinical trials across China's dynamic healthcare landscape.
🎯 Your Impact: Key Responsibilities
Clinical Trial Coordination & Management
- Work independently and actively to coordinate all activities for setting up and monitoring clinical studies
- Complete accurate study status reports and maintain comprehensive study documentation
- Run sponsor-generated queries efficiently while maintaining study cost efficiency
- Participate in preparation and review of study documentation and feasibility studies for new proposals
Site Relationship Management
- Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
- Handle site queries in a timely and professional manner using strong social skills
- Support clinical investigators and site staff throughout the trial lifecycle
- Build foundation for long-term professional relationships within China's clinical research community
Compliance & Patient Safety
- Ensure patient safety by maintaining compliance with ICON's procedures, protocols, and regulatory requirements
- Apply knowledge of ICH-GCP guidelines to daily monitoring activities
- Review and evaluate medical data with accuracy and attention to detail
- Maintain the highest standards of ethical conduct in all clinical research activities
Professional Development
- Learn clinical monitoring techniques and site management best practices
- Develop expertise in clinical trial documentation and regulatory requirements
- Build foundational skills in clinical data review and query management
- Grow into increasingly responsible clinical research roles
⭐ Your Profile: Qualifications & Experience
Essential Requirements
- University degree in medicine, science, or equivalent field
- Knowledge of ICH-GCP guidelines and ability to review medical data
- Excellent written and verbal communication skills in English and Chinese
- Good social skills enabling professional handling of site queries
Professional Attributes
- Strong organizational skills and attention to detail
- Ability to work independently while following established procedures
- Willingness to learn and develop clinical research expertise
- Professional demeanor and strong work ethic
Technical Competencies
- Basic understanding of clinical trial processes and documentation
- Ability to maintain accurate records and reports
- Computer literacy and proficiency with standard office software
- Analytical thinking for data review and problem-solving
Operational Requirements
- Ability to travel approximately 60% domestically across China
- Valid driver's license for site visit requirements
- Flexibility to adapt to changing study needs and locations
- Commitment to professional development in clinical research
💫 Why Start Your CRA Career with ICON in China?
Career Foundation
- Comprehensive training program for new CRAs entering clinical research
- Structured mentorship from experienced clinical research professionals
- Clear career progression pathway to CRA II and senior monitoring roles
- Exposure to diverse therapeutic areas and study designs
Professional Development
- Hands-on experience with leading clinical trial methodologies
- Training in ICH-GCP standards and Chinese regulatory requirements
- Development of site management and relationship-building skills
- Opportunities for professional certification and continued education
Meaningful Work
- Contribute to clinical research that addresses healthcare needs in China
- Play a role in bringing innovative treatments to Chinese patients
- Work within China's rapidly growing clinical research environment
- Join a mission-driven organization advancing global healthcare
Competitive China Benefits
- Attractive entry-level salary package with travel allowances
- Comprehensive health insurance for you and your family
- Global Employee Assistance Programme with 24/7 support
- Generous annual leave with Chinese public holidays
Career Growth Support
- Retirement planning and financial security benefits
- Life assurance coverage
- Professional development funding and training opportunities
- Health and wellness programs
- Travel and accommodation support for site monitoring
✨ Ready to Begin Your Clinical Research Journey in China?
If you're a recent graduate or early-career professional with a science or medical background and interest in clinical research, we encourage you to apply. This CRA I role offers the perfect foundation for building a successful career in clinical development while contributing to meaningful healthcare advancements across China.
Apply Now & Launch Your Clinical Research Career!
ICON is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.
We welcome applications from all qualified entry-level candidates across China - your potential and enthusiasm might be exactly what we need at ICON!
