📍 Accelerate Clinical Research as Site Activation Manager - China
Join ICON plc in China as a Site Activation Manager and lead the strategic acceleration of clinical trial site activations across this dynamic healthcare landscape. This pivotal role offers the opportunity to drive study start-up excellence while navigating China's evolving regulatory environment to bring innovative treatments to patients faster.
🎯 Your Impact: Key Responsibilities
Strategic Site Activation Leadership
- Lead end-to-end site activation processes for clinical trials across mainland China
- Develop and implement strategic site activation plans aligned with study timelines and objectives
- Navigate China's regulatory landscape including NMPA requirements and local ethics committee submissions
- Coordinate site identification, qualification, and initiation activities to ensure timely study commencement
Regulatory Excellence & Compliance
- Manage clinical trial application submissions and approvals through Chinese regulatory pathways
- Ensure compliance with Chinese GCP requirements and local regulatory standards
- Maintain current knowledge of evolving Chinese clinical trial regulations and implementation guidelines
- Prepare and submit essential documents to ethics committees and regulatory authorities
Stakeholder Management & Collaboration
- Build and maintain strong relationships with investigative sites, institutions, and key opinion leaders
- Collaborate with cross-functional teams including clinical operations, regulatory affairs, and project management
- Serve as primary point of contact for site activation activities and timeline management
- Facilitate effective communication between global study teams and local Chinese sites
Process Optimization & Timeline Management
- Implement best practices for efficient site activation and study start-up processes
- Identify and mitigate risks to site activation timelines through proactive planning
- Drive continuous improvement in site activation strategies and execution
- Monitor and report on site activation metrics and performance indicators
⭐ Your Profile: Qualifications & Experience
Essential Requirements
- Bachelor's degree in Life Sciences, Medicine, or related field; advanced degree preferred
- 5+ years of experience in clinical research with focus on site activation or study start-up in China
- Comprehensive understanding of Chinese clinical trial regulations and NMPA requirements
- Proven track record of successful site activations across multiple therapeutic areas
Regulatory Expertise
- In-depth knowledge of Chinese regulatory submission processes and timelines
- Experience with ethics committee applications and site contract negotiations
- Understanding of Chinese GCP and local implementation guidelines
- Familiarity with regulatory requirements across different Chinese provinces
Professional Competencies
- Excellent project management and timeline management skills
- Strong negotiation and relationship-building capabilities
- Ability to navigate complex regulatory and institutional environments
- Fluent in Mandarin and English with superior communication skills
Leadership Attributes
- Strategic thinker with problem-solving mindset
- Ability to work effectively in cross-cultural and cross-functional teams
- Results-oriented with focus on delivering against aggressive timelines
- Adaptable to changing regulatory landscapes and study requirements
💫 Why Join ICON in China?
Strategic Impact
- Play crucial role in accelerating clinical research in one of the world's fastest-growing healthcare markets
- Influence site activation strategies for global clinical development programs
- Build relationships with leading medical institutions and investigators across China
- Contribute to bringing innovative treatments to Chinese patients
Professional Growth
- Clear pathway to senior clinical operations and site management leadership roles
- Exposure to diverse therapeutic areas and complex study designs
- Opportunities for professional development in clinical research management
- Global networking within ICON's international site activation community
Market Leadership
- Work with world's leading clinical research organization in China's dynamic market
- Access to cutting-edge site activation technologies and processes
- Opportunity to shape site activation best practices in evolving regulatory environment
- Competitive compensation package with performance incentives
Comprehensive China Benefits
- Attractive salary package with completion bonuses
- Comprehensive health insurance for you and your family
- Global Employee Assistance Programme with 24/7 support
- Generous annual leave with Chinese public holidays
Career Development
- Retirement planning and financial security benefits
- Life assurance coverage
- Professional development allowance
- Health and wellness programs
- Transportation and commuter benefits
✨ Ready to Drive Clinical Trial Acceleration in China?
If you're an experienced site activation professional with deep knowledge of China's clinical research landscape and passion for accelerating drug development, we encourage you to apply. This Site Activation Manager role offers the unique opportunity to lead study start-up activities while contributing to clinical research that addresses healthcare needs across China.
Apply Now & Lead Site Activation Excellence in China!
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 site activation professionals across China - your regulatory expertise and site relationship management skills might be exactly what we need at ICON!
