Clinical Study Coordinator (Technical Officer/Research Assistant I/II)

Job Description

Main Responsibilities:

Undertake clinical trial coordination and operations responsibilities, including but not limited to plan and manage studies;
Develop and maintain of clinical studies’ database using the eSource and site automation solution, AnjuEPS;
Perform study procedures, data collection, documents management, facilities management and quality management; and
Communicate with research teams and internal/external collaborators.
Working outside normal business days or hours may be required occasionally.

Requirements:

Bachelor’s degree in Biological, Medical, Life Sciences or equivalent;
Some experience in clinical research and basic knowledge in Good Clinical Practice (GCP) are added advantages;
Good coordination and problem-solving skills, good interpersonal and communication skills, and commitment to quality and compliance;
Detail-minded, able to handle multiple concurrent tasks, and self-motivated;
Good command of written and spoken English and Chinese.
A highly competitive salary commensurate with qualifications and experience will be offered, in addition to annual leave and medical benefits. The appointment will commence as soon as possible for one or two years, renewable subject to satisfactory performance. Appointment on two-year fixed term will attract a contract-end gratuity and University contribution to a retirement benefits scheme, totalling up to 10% of basic salary.

The University only accepts online application for the above post. Applicants should apply online at the University’s career site (https://jobs.hku.hk) and upload an up-to-date C.V.  Review of applications will start from November 15, 2024 and continue until December 1, 2024 or until the post is filled, whichever is earlier.