Clinical Medical Manager
Time：2025-07-07

Responsibilities

1.Participated in the drafting of clinical trial protocols, investigator manuals, informed consent forms, and research medical records, etc.

2. Responsible for the collection, organization and analysis of medical information, and supporting the formulation of marketing strategies;

3. Based on the opinions of the PI, the ethics committee, the medical director, the project monitoring department, etc., the medical data were revised.

4. Track the efficacy and safety data, and review the clinical research reports.

5. The review plan ensures consistency with the operation, in order to guarantee the medical compliance of the plan.

6. Regularly update the medical knowledge base to ensure the timeliness and accuracy of the information.

7. Assist in the operation management of clinical projects;

Qualifications

1. Master's degree or above in fields such as medicine, pharmacy, oncology, molecular biology, etc.

2. Possess at least one year of work experience in the medical field. Those who have participated in the entire process of the first-phase clinical project for tumors will be given priority.

3. Medical professionals who have participated in the development of innovative drugs in the field of immunotherapy will be given priority.

4. Excellent communication skills and teamwork spirit;

5. Proficient in using office software, with strong skills in document editing and report writing;

6. Possess strong learning ability and be able to quickly master new knowledge and skills;

7. Fluent in English speaking, listening, reading and writing, capable of reading English literature;

8. Possessing excellent professional ethics and qualities, and being able to cope with certain levels of work pressure.

E-mail：hr@kangabio.com