CRA Job at ICON, Taiwan | Life Sciences | Clinical Site Associate (In-House CRA) | Apply Now
If you are looking to build a strong foundation in clinical trial operations and site management, this Clinical Site Associate (In-House CRA) position with ICON plc in Taipei is a stellar opportunity. Operating as an essential bridge between external clinical sites and internal project teams, this CRA Job serves as the perfect entry or early-career stepping stone into the world of clinical monitoring. For those seeking a dynamic, fast-paced clinical research job, this role offers the perfect environment to learn the mechanics of study start-up and launch a long-term ICON career.
About the Company
ICON plc is a world-leading healthcare intelligence and clinical research organization (CRO) dedicated to shaping the future of global clinical development. ICON is deeply committed to inclusion, belonging, and nurturing internal talent. They prioritize building a diverse workforce that rewards high performance and encourages continuous professional development. As a full-service CRO, ICON supports the biotechnology, pharmaceutical, and medical device industries across the globe, giving you exposure to top-tier, international clinical trials.
CRA Job – Key Responsibilities
As a Clinical Site Associate, you will play a critical, central role in supporting site management activities, ensuring that clinical trials are conducted efficiently, compliantly, and to the highest quality standards.
Your day-to-day operational and administrative duties will include:
- Study Start-Up & Activation: Supporting critical site activation activities, including the collection, thorough review, and precise tracking of essential regulatory documents and approvals.
- CTMS Maintenance: Maintaining up-to-date site information, enrollment tracking, and trial status within the Clinical Trial Management Systems (CTMS) and internal trackers.
- CRA Coordination: Assisting field-based Clinical Research Associates (CRAs) and project teams with site communications, active follow-ups, and the rapid resolution of site-level queries.
- Logistical Support: Coordinating logistics for essential site visits and meetings, which includes scheduling, preparing necessary documentation, and tracking follow-up actions.
- Audit Readiness: Ensuring the highly accurate filing and maintenance of essential documents in the Trial Master File (TMF) to support constant inspection and audit readiness.
- Financial Processing: Collaborating with internal stakeholders to support timely site payment processing and the resolution of any financial issues.
- Process Optimization: Actively contributing to process improvement initiatives and sharing best practices to enhance the overall efficiency of site support.
Qualifications & Skills Required For CRA Job
This clinical research job is perfectly tailored for organized, detail-oriented professionals eager to support complex project workflows.
- Educational Foundation: A Bachelor’s degree in Life Sciences, Healthcare, Business, or a related field (or equivalent professional experience).
- Preferred Experience: Initial, foundational experience in clinical research, clinical administration, or a similarly highly regulated environment is strongly preferred.
- Organizational Mastery: Strong organizational skills with the proven ability to seamlessly manage multiple tasks, shifting priorities, and strict deadlines.
- Technical & Soft Skills: High proficiency with MS Office and a strong comfort level navigating electronic systems and complex databases.
- Communication Fluency: Effective written and verbal communication skills paired with a highly customer-focused approach to supporting trial site staff.
- Mindset: High attention to detail, accuracy in documentation, and the flexibility to work collaboratively within a team environment adapting to changing project priorities.
Logistics, Compensation & Total Rewards
- Location: Taipei, Taiwan. (The role specifies alignment with the ICON Taipei office, with remote or office-based flexibility depending on final team structure).
- Job Function: Clinical Monitoring / Full Service & Corporate Support.
- Health & Wellness: A range of health insurance offerings tailored to suit you and your family’s needs, alongside standard life assurance policies.
- Financial Planning: Competitive retirement planning offerings designed to maximize your savings so you can plan with confidence for the years ahead.
- Employee Assistance: Access to the Global Employee Assistance Programme (LifeWorks), offering 24-hour access to a network of over 80,000 independent, specialized professionals.
- Work-Life Balance: Various competitive annual leave entitlements and flexible country-specific optional benefits to support a healthy work-life balance.
In summary, this Clinical Site Associate position is an outstanding entry point into the highly competitive clinical monitoring landscape. By securing this CRA Job, you will master the essential documentation, payment, and coordination processes that keep global clinical trials moving forward. If you have a relevant degree, a meticulous eye for detail, and the drive to improve patient care, apply today to secure this premier clinical research job and fast-track your ICON career.
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