Clinical Research Associate – Taiwan

About the role

The Clinical Research Associate (CRA) will support the execution of clinical trials across selected sites in Taiwan. You will ensure that each study is conducted in compliance with the protocol, ICH‑GCP, and local regulations while maintaining high standards of data quality and patient safety.

Key responsibilities

• Identify and qualify study sites, conduct site initiation visits (SIV) and provide ongoing training on protocol and GCP requirements.
• Perform routine monitoring visits, source‑data verification, and issue resolution, documenting findings in timely monitoring reports.
• Coordinate the delivery of study materials (drug, equipment, CRFs) and manage site-specific ethics committee submissions.
• Oversee safety reporting, ensuring adverse events are reported within required timelines.
• Manage site budgets, contracts, and payment schedules, retaining all relevant documentation.
• Maintain study tools and systems, ensuring data integrity throughout the trial lifecycle.

Required profile

• Bachelor’s degree or higher in Medicine, Pharmacology, Biology or a related field.
• Minimum of 1 year of experience as a CRA or in clinical trial monitoring.
• Solid understanding of Good Clinical Practice (GCP) and clinical trial operations.
• Proficient written and spoken English.

Required skills

What we offer

• Opportunity to work on international clinical studies.
• Professional development in a dynamic, compliance‑focused environment.