Job Description.

1. Search and read literature, learn clinical research background and trial protocols, assist in the design and writing of trial protocols and project approval documents.

2. Responsible for appropriate medical support during project development and clinical studies.

3. Facilitate and assist in clinical trials.

4. Analyse and collate test data and write reports.

5. Maintains professional communication with clinical experts and national drug evaluation authorities during all phases of device development projects.

6. Mentor team members to improve their professional competence and professionalism.

Job Requirements.

1. Master's degree or above in clinical medicine.

2. Three years of medical support or related work experience, preferably in device development and clinical evaluation.

3. Ability to adapt to short-term overtime and business travel.

4. Good command of English.

5. Team player, good organisational, communication and coordination skills and strong initiative.