
Clinical Research Associate I/II/Senior
Posted Jun 3

Posted Jun 3
This is a fully remote position, open to applicants in Taiwan.
• Assists in identifying potential investigators
• Oversees and finalizes study sites while adhering to Client Procedural Documents
• Updates the Clinical Trial Management System (CTMS) and other platforms with data from study sites according to specified timelines
• Conducts monitoring visits, both remotely and onsite
• Collaborates with data management to ensure high quality of the collected study data
• Prepares and completes monitoring visit reports
• Bachelor’s degree in a related field, ideally in life sciences, or an equivalent qualification
• Strong attention to detail
• Effective written and verbal communication skills
• Proficiency in both written and spoken English is essential
• Fluency in local language(s) is required
• Comprehensive understanding of international guidelines such as ICH-GCP
• Basic knowledge of Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP)
• Familiarity with pertinent local regulations
• Opportunities for professional development
Parexel
ICON plc
Precision Medicine Group
Worldwide Clinical Trials
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