1. Responsible for conducting clinical tests on our products and communicating with the external world.

2. Cooperate with the PDO project to apply for product registration.

3. Give assistance to complete relevant product research and development of the company in terms of examination, evaluation, laws and regulations. 

1. Have experience in registration of in vitro diagnostic reagents, be familiar with relevant procedures and independently conduct clinical tests and relevant application work. 

2. Have a relevant research and development background, be familiar with research and development of in vitro diagnostic reagents and have experience in successful products.

3. Hold a Master's Degree or above and have over two years of relevant work experience.