职位描述：
responsibilities:
1. independently undertake and fully take charge of all clinical trials of the company;
2. responsible for the experimental design, business communication and implementation plan of clinical efficacy, pharmacokinetics, safety evaluation and other related researches, and ensure that the experimental projects are carried out in strict accordance with the program, sop and relevant laws and regulations;
3. responsible for the implementation and supervision of various clinical trials, and completed all clinical trials with high quality and efficiency;
4. responsible for negotiation, coordination and supervision of clinical trial contracts;
5. responsible for finishing the sorting of clinical data in project registration and assisting in project application.
job requirements:
1. with medical background, master degree or above in clinical medicine or clinical pharmacy;
2. strong executive ability, sense of responsibility, active thinking, innovation and teamwork spirit;
3. at least 3 years of project manager or cro medical department manager experience;
4. good at english, proficient in translation and writing of professional foreign language documents; organize related materials, have strong writing skills and english communication skills;
5. familiar with gcp and other clinical trial regulations and international registration regulations, capable of carrying out relevant training and quality control.