Responsibilities

• Lead the clinical research study focusing on eye disorder in children and adolescents;
• Monitor and ensure the fidelity of implementation for randomized control trials (RCTs), maintaining adherence to study protocols and methodologies;
• Contribute to data entry, data cleaning, and conduct statistical analyses, including data visualization and interpretation.
  
  
  

Qualifications

• Possess a Bachelor’s degree or above in health science-related degrees. A doctoral degree is a plus;
• Proficiency in statistical software (SAS, STATA, or R) is required;
• Demonstrated knowledge and work experience in the design, conduct, and analysis of RCTs are desirable;
• Ability to work independently across multiple protocols, sites, and therapy areas;
• Excellent interpersonal skills and ability to interact with diverse internal and external collaborators;
• Experience applying English- and Chinese-language written and oral communication skills to research studies and make effective presentations;
• Publication in peer-reviewed medical journals is preferred.
  
  
  

A highly competitive salary commensurate with qualifications and experience will be offered, in addition to annual leave and medical benefits. Applicants should apply and attach an application letter and a detailed resume stating their current and expected salary. Review of applications will continue until the post is filled, whichever is earlier.

We are an equal opportunities employer and welcome applications from all qualified candidates.

All applications applied through our system will be delivered directly to the advertiser and privacy of personal data of the applicant will be ensured with security.