🚀 Launch Clinical Trials as Study Start Up Associate - Taiwan
Join ICON plc in Taiwan as a Study Start Up Associate and be at the forefront of initiating groundbreaking clinical trials. This client office-based role with flexible work-from-home options offers the perfect entry point into clinical research, where you'll help accelerate the start of vital studies that bring innovative treatments to patients across Taiwan.
🎯 Your Impact: Key Responsibilities
Regulatory Documentation & Submissions
- Assist in preparation and submission of regulatory documents including clinical trial applications and ethics committee submissions
- Maintain accurate and up-to-date records of all regulatory submissions and approvals
- Support the development of essential study documents including protocols, informed consent forms, and investigator brochures
- Ensure all documentation meets Taiwanese regulatory standards and timelines
Stakeholder Coordination & Collaboration
- Coordinate with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation
- Participate in study start-up meetings, providing valuable input on regulatory requirements and timelines
- Collaborate effectively with cross-functional teams including clinical operations, regulatory affairs, and project management
- Build relationships with ethics committees and regulatory authorities across Taiwan
Process Management & Compliance
- Manage multiple tasks simultaneously in a fast-paced clinical research environment
- Ensure compliance with Taiwanese regulatory requirements and ICON quality standards
- Support continuous improvement of study start-up processes and documentation
- Maintain organized tracking systems for submission milestones and approvals
Study Initiation Support
- Contribute to the successful and timely initiation of clinical trials across Taiwan
- Learn and apply regulatory knowledge to accelerate study start-up timelines
- Support site activation activities and preparatory work for clinical trial commencement
- Develop expertise in Taiwan-specific clinical trial regulations and requirements
⭐ Your Profile: Qualifications & Experience
Essential Requirements
- Bachelor's degree in life sciences or related field
- Strong attention to detail and exceptional organizational skills
- Excellent communication and interpersonal skills in Chinese and English
- Ability to work independently and manage multiple tasks in fast-paced environment
Preferred Qualifications
- Previous experience in clinical research or regulatory affairs (not required)
- Understanding of clinical trial processes and regulatory requirements in Taiwan
- Familiarity with clinical trial documentation and submission processes
- Interest in pharmaceutical development and clinical research
Professional Attributes
- Quick learner with strong problem-solving capabilities
- Collaborative team player with cross-functional engagement skills
- Proactive approach to task management and timeline adherence
- Adaptable to changing priorities and study requirements
Work Arrangement
- Comfortable with client office-based work and flexible WFH arrangement
- Ability to balance in-person collaboration with remote work efficiency
- Self-motivated with strong time management in hybrid work setting
- Willing to learn and grow in dynamic clinical research environment
💫 Why Join ICON in Taiwan?
Career Launchpad
- Perfect entry point for starting a career in clinical research
- Comprehensive training and mentorship program
- Clear pathway to advanced study start-up and regulatory roles
- Exposure to global clinical development processes
Meaningful Impact
- Contribute to bringing innovative treatments to Taiwanese patients
- Play a crucial role in accelerating clinical trial initiation
- Support medical advancements that improve patient outcomes
- Work at the forefront of Taiwan's growing clinical research landscape
Flexible Work Environment
- Client office-based position with flexible work-from-home options
- Supportive team environment with experienced mentors
- Modern workplace with collaborative atmosphere
- Balance of structured office work and remote flexibility
Professional Development
- Learn Taiwanese regulatory requirements and submission processes
- Develop expertise in clinical trial documentation and compliance
- Gain exposure to multiple therapeutic areas and study designs
- Access to ICON's global training and development resources
Competitive Taiwan Benefits
- Attractive entry-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 Taiwanese public holidays
Additional Benefits
- Retirement planning and financial security benefits
- Life assurance coverage
- Professional development funding and training opportunities
- Health and wellness programs
- Transportation support and commuter benefits
✨ Ready to Launch Your Clinical Research Career in Taiwan?
If you're a life sciences graduate with strong organizational skills and interest in clinical research, we encourage you to apply. This Study Start Up Associate role offers the perfect foundation for building a successful career in clinical development while enjoying the flexibility of client office-based work with work-from-home options in Taiwan.
Apply Now & Start Your Clinical Research Journey!
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 Taiwan - your potential and enthusiasm might be exactly what we need at ICON!
