Clinical Research Associate – SM
Posted May 25
Posted May 25
This is a fully remote position, open to applicants in Taiwan.
• You will play a key role in monitoring clinical trial activities, taking ownership of your deliverables and collaborating effectively with the team.
• Conduct site qualification, initiation, monitoring, and closure visits for clinical trials.
• Ensure compliance with protocols, maintain data integrity, and prioritize patient safety throughout the trial.
• Work alongside investigators and site personnel to ensure seamless study execution.
• Perform data review and resolve queries to uphold the quality of clinical data.
• Assist in the preparation and evaluation of study documents, including protocols and clinical study reports.
• Bachelor's degree in a scientific or healthcare-related discipline.
• At least 2 years of experience as a Clinical Research Associate.
• Comprehensive knowledge of clinical trial processes, relevant regulations, and ICH-GCP guidelines.
• Excellent organizational and communication skills, with a strong attention to detail.
• Capability to work both independently and collaboratively in a dynamic environment.
• Willingness to travel as necessary (approximately 60%).
• Various annual leave entitlements.
• A range of health insurance options tailored to meet you and your family’s needs.
• Competitive retirement planning options to maximize savings and prepare confidently for the future.
• Global Employee Assistance Programme, TELUS Health, providing 24-hour access to a worldwide network of over 80,000 independent specialized professionals dedicated to supporting your and your family’s well-being.
• Life assurance.
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Parexel
ICON plc
Precision Medicine Group
Worldwide Clinical Trials
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