Responsibilities
• Oversee the smooth conduct of clinical trials
• Handle daily activities as described in study protocols including clinical measurements and processing study specimens
• Manage communication with study subjects, investigators, sponsors and other clinical research stakeholders
• Ensure high quality of work meeting Good Clinical Practice (GCP) and other applicable regulatory requirements
• Participate in outreach activities for recruitment purpose
• May be involved in other study-related activities e.g. data-mining, social media design

Requirements
• Degree or above in the medical sciences, nursing or related fields
• Work experience in clinical research or clinical trials for at least 2 years
• Good knowledge of ICH/GCP requirements
• Proficiency in both written and spoken English and Chinese (including Cantonese & Putonghua)
• Attention to details and analytical mindset

We offer competitive remuneration packages.

Applicants are to send their resume, with contact... details to us or by clicking apply now.

Personal data collected will be used for recruitment purposes only
Central Hong Kong

Salary Criteria