š Launch Your Clinical Research Career in China
JoinĀ ICON plcĀ as anĀ In-House Clinical Research AssociateĀ in either Beijing or Shanghai, and begin your journey in clinical research with a global leader. This office-based role offers the perfect foundation for building your career, providing comprehensive exposure to clinical trial operations while working from our modern offices in China's most dynamic cities.
šÆ Your Impact: Key Responsibilities
Clinical Trial Support
- Assist in planning, initiating, and executing clinical trial activities
- Conduct site feasibility assessments and support site selection processes
- Coordinate with investigative sites to ensure protocol compliance
- Monitor study progress and data collection activities
Documentation & Compliance
- Support preparation and review of study documentation and reports
- Help ensure compliance with regulatory requirements and ICON SOPs
- Assist with essential document collection and tracking
- Support Trial Master File (TMF) management
Site Management Assistance
- Serve as key in-house contact for clinical sites
- Facilitate communication between sites and study teams
- Track site performance and enrollment metrics
- Support resolution of site queries and issues
Operational Excellence
- Maintain study timelines and tracking systems
- Participate in team meetings and training sessions
- Support quality control and process improvement initiatives
- Assist with regulatory submission preparations
ā Your Profile: Qualifications & Experience
Essential Requirements
- Bachelor's degree in Life Sciences, Healthcare, or related field
- Understanding of clinical research principles andĀ ICH-GCP guidelines
- Fluency in English and MandarinĀ (written and verbal)
- Strong organizational and communication skills
- Ability to work in fast-paced, office-based environment
Ideal Candidate Profile
- Previous exposure to clinical research or healthcare environment
- Excellent attention to detail and task prioritization skills
- Strong computer literacy and quick learner of new systems
- Professional demeanor and collaborative mindset
Key Attributes
- Proactive problem-solving approach
- Excellent interpersonal and relationship-building skills
- Ability to work both independently and in team settings
- Commitment to quality and process improvement
š« Why Join ICON in China?
Career Foundation
- Comprehensive training program for IHCRA role
- Clear career progression path to CRA and beyond
- Mentorship from experienced clinical research professionals
- Exposure to global clinical trials and processes
Office Environment
- Modern, professional workplaces in Beijing or Shanghai
- Collaborative team culture with global connectivity
- Structured office-based schedule with work-life balance
- Opportunities for continuous learning and development
Competitive Benefits
- Attractive entry-level salary package
- Comprehensive health insurance coverage
- Retirement planning and financial security programs
- Generous vacation entitlements and wellness support
- Professional development opportunities
āØ Ready to Start Your Clinical Research Journey?
If you're looking to begin a meaningful career in clinical research and have the basic qualifications we're seeking, we encourage you to apply. We value potential and dedication - your attitude and willingness to learn are just as important as your existing experience!
Apply Now & Build Your Future in Clinical Research
