We are currently working with a leading global Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. They are currently in search of a Clinical Research Associate with experience in Oncology. 

As a Clinical Research Associate you will: 

• Conduct and report all types of onsite monitoring visits
• Be involved in study startup and feasibility research
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Be a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress
• Support regulatory team in preparing documents for study submissions

As a Clinical Research Associate you will need: 

• College/University degree in Life Sciences or an equivalent combination of education, training & experience 2 years of independent on-site monitoring experience in the Hong Kong required Independent monitoring experience in Hong Kong and knowledge of the local clinical research environment
• Experience in all types of monitoring visits in Phase II / III Therapeutic area experience in at least one of PSI key areas: oncology, gastroenterology
• Full working proficiency in English for MS Office applications
• Ability to plan and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills Ability to travel