✍️ Lead Scientific Communication as Senior Medical Writer - Shanghai/Beijing
Join ICON plc in China as a Senior Medical Writer and become the architect of compelling scientific narratives that drive clinical development forward. This pivotal role in Shanghai or Beijing offers the opportunity to shape medical communication strategies while mentoring the next generation of scientific writers in China's dynamic healthcare landscape.
🎯 Your Impact: Key Responsibilities
Strategic Document Development
- Lead preparation, review, and editing of comprehensive clinical documents including protocols, clinical study reports, investigator brochures, and regulatory submissions
- Ensure all documents demonstrate accuracy, clarity, and compliance with Chinese and international regulatory standards
- Provide strategic input for clinical development programs, supporting study design and interpretation
- Develop publication plans and create abstracts, posters, and manuscripts for leading scientific journals
Scientific Interpretation & Communication
- Collaborate with cross-functional teams to interpret complex clinical trial data and statistical analyses
- Transform scientific findings into clear, compelling narratives for diverse audiences
- Communicate key insights through well-structured regulatory documents and scientific publications
- Maintain scientific integrity while ensuring regulatory compliance across all written materials
Team Leadership & Mentorship
- Mentor and coach junior medical writers in best practices, writing techniques, and scientific principles
- Foster a culture of excellence, collaboration, and continuous learning within the medical writing team
- Provide guidance on China-specific regulatory requirements and international standards
- Share expertise in therapeutic areas and clinical development methodologies
Regulatory Expertise
- Navigate complex regulatory landscapes including NMPA, FDA, EMA, and ICH-GCP requirements
- Support interactions with regulatory agencies during document review and approval processes
- Ensure all submissions meet both global standards and China-specific regulatory expectations
- Stay current with evolving regulatory guidelines and industry best practices
⭐ Your Profile: Qualifications & Experience
Educational Foundation
- Advanced degree in Life Sciences, Pharmacy, Medicine, or related field
- 3-5 years of medical writing experience in pharmaceutical, biotechnology, or CRO industry
- Strong academic background with demonstrated scientific writing capabilities
Technical Expertise
- Proficiency in interpreting and summarizing complex clinical trial data and statistical analyses
- Excellent writing, editing, and proofreading skills with attention to detail
- Ability to communicate scientific concepts effectively to diverse audiences
- Experience with regulatory document preparation and submission processes
Regulatory Knowledge
- Strong understanding of NMPA, FDA, EMA, and ICH-GCP requirements
- Experience interacting with regulatory agencies during review processes
- Knowledge of clinical document preparation standards and publication guidelines
- Familiarity with China-specific regulatory landscape and requirements
Professional Competencies
- Ability to manage multiple projects in fast-paced, deadline-driven environment
- Excellent interpersonal and communication skills in Chinese and English
- Strong collaboration capabilities with cross-functional teams
- Leadership skills with ability to mentor and influence stakeholders
💫 Why Join ICON in China?
Strategic Impact
- Play crucial role in bringing innovative treatments to Chinese patients
- Shape medical communication strategies for groundbreaking clinical research
- Influence regulatory submissions and scientific publications
- Contribute to China's growing presence in global clinical development
Professional Growth
- Clear pathway to Medical Writing leadership and directorship roles
- Exposure to diverse therapeutic areas and complex study designs
- Opportunities for professional development and advanced training
- Global networking within ICON's worldwide medical writing community
Location Advantages
- Choice of Shanghai or Beijing - China's leading healthcare and research hubs
- Access to cutting-edge clinical research and scientific communities
- Professional workplace environments with modern facilities
- Vibrant cities with rich cultural and professional opportunities
Competitive China Benefits
- Attractive senior-level salary package with performance incentives
- 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 and training opportunities
- Health and wellness programs
- Transportation support and commuter benefits
✨ Ready to Shape Medical Communication in China?
If you're an experienced medical writer with passion for scientific communication and regulatory excellence, we encourage you to apply. This Senior Medical Writer role offers the unique opportunity to lead document development while contributing to clinical research that advances healthcare in China and worldwide.
Apply Now & Lead Our Medical Writing 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 medical writing professionals in Shanghai and Beijing - your scientific communication expertise might be exactly what we need at ICON!
