Freelance Clinical Research Associate CRA - Hong Kong

Our client is a reputable Contract Research Organization (CRO) is seeking a freelance/contract CRA based in Hong Kong for a pediatric study.

Estimated FTE: 0.30.4

Key Responsibilities:

Conduct site selection feasibility and site activation procedures including ethics submissions regulatory document/ICF review and site contract negotiation
Conduct site selection site initiation interim monitoring and close out visits
Conduct all clinical site activities according to the monitoring plan and in accordance with the study timelines

Review and Approve site payments
May take on Project Management tasks
Participate in and respond to clinical trial audits

Requirements:

• Bachelors Degree or above in associated field.
• Excellent communication and interpersonal skills.
• 4 years of independent onsite monitoring in a pharmaceutical biotech or CRO environment
• Strong knowledge of GCP national and international guidelines.
• Strong knowledge of Hong Kong Ethics Committee submission process
• Proficient in written Chinese and spoken Cantonese