🏥 Advance Clinical Research in Taiwan: CRA (All Levels) - Home-Based
Join ICON plc as a Clinical Research Associate in Taiwan and become the driving force behind groundbreaking medical studies from the comfort of your home. This home-based role offers opportunities across all experience levels, allowing you to grow your career while overseeing clinical trials that improve healthcare outcomes across Taiwan and beyond.
As a world-leading healthcare intelligence organization, we're seeking dedicated CRAs at various career stages to monitor and coordinate clinical trials throughout Taiwan. If you're passionate about clinical research and seek flexible home-based work with extensive field travel, this is your opportunity to build a meaningful career while contributing to medical advancements that benefit Taiwanese patients.
🎯 Your Clinical Research Mission: Key Responsibilities
Clinical Trial Coordination & Monitoring
- Work independently to coordinate all activities for study setup and ongoing monitoring
- Complete accurate study status reports and maintain comprehensive study documentation
- Run sponsor-generated queries efficiently while ensuring study cost efficiency
- Ensure patient safety through strict compliance with protocols and regulatory requirements
Site Management & Relationship Building
- Develop and maintain strong, collaborative relationships with clinical investigators and site staff
- Conduct site visits to monitor protocol compliance, data quality, and patient safety
- Provide training and support to site staff on study procedures and requirements
- Serve as primary point of contact for assigned clinical trial sites across Taiwan
Documentation & Regulatory Compliance
- Participate in preparation and review of study documentation and feasibility studies
- Ensure all activities comply with ICH-GCP guidelines and Taiwan regulatory requirements
- Maintain audit-ready documentation for all monitoring activities and site communications
- Support regulatory submissions and inspections as required
Study Efficiency & Quality Assurance
- Implement quality control measures to ensure data integrity and protocol adherence
- Identify and resolve site issues proactively to maintain study timelines
- Contribute to process improvement initiatives for enhanced study efficiency
- Support study close-out activities including data reconciliation and document archiving
⭐ Your Profile: Clinical Research Capabilities
Essential Qualifications
- University degree in Medicine, Science, or equivalent healthcare field
- Knowledge of ICH-GCP guidelines and ability to review medical data
- Excellent written and verbal communication in English and Mandarin
- Valid driver's license and willingness to travel extensively (minimum 60%)
Experience Levels We Welcome
- Entry-Level CRA: New graduates or professionals transitioning to clinical research
- Junior CRA: 1-2 years clinical research or site coordination experience
- CRA II: 2-4 years direct monitoring experience in Taiwan
- Senior CRA: 4+ years comprehensive monitoring experience with leadership skills
Professional Attributes
- Strong Social Skills: Ability to handle queries and build relationships effectively
- Independent Work Ethic: Capability to work autonomously with minimal supervision
- Attention to Detail: Meticulous approach to documentation and compliance
- Adaptability: Flexibility to manage multiple priorities in dynamic environment
Travel Requirements
- Ability to travel minimum 60% across Taiwan (domestic and potentially international)
- Comfort with fly-and-drive assignments to various clinical sites
- Flexibility for extensive travel throughout Taiwan's healthcare institutions
- Willingness to visit hospitals and research centers across different regions
💫 Why Build Your CRA Career at ICON Taiwan?
Impact Healthcare in Taiwan
- Contribute to clinical trials bringing innovative treatments to Taiwanese patients
- Work with leading medical institutions and investigators across Taiwan
- Ensure research quality that meets international standards and regulatory requirements
- Play crucial role in advancing medical science in Taiwan's growing research landscape
Home-Based Flexibility with Field Impact
- 100% home-based work with comprehensive technology support
- Extensive travel across Taiwan's clinical research sites and hospitals
- Balance autonomous home office work with meaningful field engagement
- Professional setup with IT infrastructure for seamless virtual collaboration
Career Growth Across Levels
- Structured progression from entry-level to senior monitoring roles
- Comprehensive training program tailored to experience level
- Opportunities for therapeutic area specialization
- Professional development within global clinical research organization
Competitive ICON Taiwan Benefits
- Attractive salary package with performance incentives
- Comprehensive health insurance for you and your family
- Global Employee Assistance Programme with local support
- Generous annual leave with Taiwanese public holidays
- Retirement planning benefits and financial security
- Travel allowance and expense coverage for site monitoring
- Professional development allowance and certification support
🏥 Therapeutic Areas You'll Impact
- Oncology and Hematology
- Cardiology and Metabolic Diseases
- Neurology and Psychiatry
- Infectious Diseases and Vaccines
- Rare Diseases and Specialized Therapies
🗺️ Travel Coverage Across Taiwan
- Northern Taiwan (Taipei, New Taipei, Taoyuan)
- Central Taiwan (Taichung, Changhua, Nantou)
- Southern Taiwan (Tainan, Kaohsiung, Pingtung)
- Eastern Taiwan (Hualien, Taitung)
- Offshore Islands (Penghu, Kinmen, Matsu)
✨ Ready to Advance Clinical Research in Taiwan?
Whether you're beginning your clinical research journey or are an experienced monitoring professional, we encourage you to apply. These CRA roles offer unique opportunities at all career levels to contribute to groundbreaking research while enjoying home-based flexibility across Taiwan.
Apply Now and become ICON's next Clinical Research expert in Taiwan!
