We are seeking a Clinical Research Associate (CRA) to support an oncology clinical study in Hong Kong.

• Location: Hong Kong 
• Full-Time

This role involves monitoring, site management, and regulatory compliance to ensure study integrity and patient safety.

Key Responsibilities:

• Conduct site visits, monitoring, and data verification.
• Ensure compliance with GCP, protocols, and regulatory requirements.
• Collaborate with investigators and site staff to ensure study progress.
• Maintain accurate documentation and reporting.

Requirements:

• Degree in life sciences or related field.
• 2 years of CRA experience (oncology preferred).
• Strong knowledge of GCP and regulatory guidelines.
• Fluent in Mandarin and/or Cantonese (spoken and written).
• Excellent communication and organizational skills.

Apply now