Clinical Development, Lead

Job Description:

1. In charge of protocol design and implementation for early stage drug development;

2. Provide input to preclinical data during IND preparation via leading internal and external discussion and drive decision making regarding study protocol and sequential clinical strategy;

3. Identify compounds’ strengths by cooperating with other functional teams in order to translate preclinical data to clinical output;

4. Pursuing clinical and regulatory expertise externally to ensure protocol quality from clinical science and regulatory perspectives;

5. Provide clinical expertise via interacting with other functional teams for selecting/deciding research direction or new project;

6. Team management, training and etc.

Job Requirements:

1. Master’s degree or above;

2. Clinical medicine and pharmacology background;

3. Work experiences:

(1) Physician-in-charge and Master’s degree in areas of tumor, endocrine, cardiovascular, blood, neurological diseases and etc.;

(2) Major in clinical medicine or other related professionals, has Phase I clinical protocol design experiences in tumor, diabetes hepatitis and other disease areas; or has experiences in early stage clinical development in pharmaceutical industry/academia in preferred;

4. Qualifications:

(1) Strong knowledge background in clinical medicine and clinical pharmacology, and sufficient early stage clinical development experience in tumor, diabetes hepatitis and other disease;

(2) Ability to analyze and judge the literature and results of research;

(3) Familiar with the basic procedure of drug development and related policies and regulations;

5. Professional accomplishment: Positive, Dedicated, initiative, responsible and rightful;

6. Language skills: excellent Chinese and English skills in reading and