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 to be part of an impactful oncology research team!
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